Convertors

Surgical Pack Procedure Mayo Stand Cover TOWELX5 Suture BAG HEAD/SIDEX2/FOOT Sheet Outer/Wrap Table Cover Sterile

Registry build 21.09.26
24manufacturers in China registered for this device type
183catalogue numbers in this listing
26recalls on this code

Who Else Makes It

Concentrated in Jiangsu (11), Anhui (6), Zhejiang (4). 9 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LRO
Manufacturer City Province Registered as Device types
Conod Medical Co., Limited Changshu Jiangsu Contract manufacturer 48
Principle & Will Biotech (Pinghu) Co., Ltd. Pinghu Zhejiang Contract manufacturer 39
Sino Protection (Hefei) Medical Products Co., Ltd. Hefei Anhui Contract manufacturer 18
Changzhou Holymed Products Co., Ltd. Changzhou Jiangsu Contract manufacturer 16
Donghai Xingchen NON-Woven Products Co., Ltd. North Donghai Development Zone, Lianyungang Jiangsu Contract manufacturer 7
Fengyang Jiehong Nonwoven Product Co., Ltd. Chuzhou Anhui Contract manufacturer 7
3A Medical Products Co., Ltd. Liu An Anhui Contract manufacturer 6
Cobes Industries (Jinzhai) Co., Ltd. Luan Anhui Contract manufacturer 6
Lianyungang Aiyeh Non-woven Products Co., Ltd. Lianyungang Jiangsu Contract manufacturer 6
Jiangsu NEW Pentastar Medical Products Co., Ltd. Changzhou Jiangsu Exporter 146
Ningbo Greetmed Medical Instruments Co., Ltd. Ningbo Zhejiang Specification developer 75
GRI Medical & Electronic Technology Co., Ltd. Jiaxing Zhejiang Contract manufacturer 71

Showing 12 of 24. All 24 manufacturers in China registered for General Surgery Tray

Record

Regulatory record for Convertors
Listed by Cardinal Health 200, LLC, United States
FDA product code LRO
Device type General Surgery Tray
Device class Class 2
Regulation 21 CFR 878.4370
Establishment Contract manufacturer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2016-07-14
Record revised 2022-06-17 (version 8)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Ethylene Oxide
Supplied sterile Yes
Single use Yes
Over the counter Yes
Supplied as a kit Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Packaging Case of 6, case of 10, case of 5, case of 8, case of 4, case of 3
Distribution end date 2027-11-05

Catalogue Numbers

Catalogue numbers for Convertors
Catalogue number Size Per pack Status
9102 In distribution
29130 In distribution
29490 In distribution
29480 In distribution
29606 In distribution
9112 In distribution
29107 In distribution
9150 In distribution
9113 In distribution
9599 In distribution
29127 In distribution
95995 In distribution
9111 In distribution
29189 In distribution
29131 In distribution
29107 In distribution
9541 In distribution
29604 In distribution
29180 In distribution
29471 In distribution
29365 In distribution
9520E In distribution
29138 In distribution
9113 In distribution
29503 In distribution
9041 In distribution
29188 In distribution
29245 In distribution
117 In distribution
9545 In distribution
29133 In distribution
29242 In distribution
9511 In distribution
29188 In distribution
9120 In distribution
9165 In distribution
9103 In distribution
29133 In distribution
29408 In distribution
29138 In distribution
29480 In distribution
29118 In distribution
9150 In distribution
9520E In distribution
TB29118 In distribution
29171 In distribution
29606 In distribution
29181 In distribution
9419 In distribution
9102 In distribution
9111 In distribution
9120 In distribution
9274 In distribution
29182 In distribution
29490 In distribution
9153N 5 In distribution
9106 In distribution
29130 In distribution
29131 In distribution
29120 In distribution
9183 In distribution
29471 In distribution
9419 In distribution
9100 In distribution
29242 In distribution
29187 In distribution
9194 In distribution
9196 In distribution
9440 In distribution
29127 In distribution
9101 In distribution
77000 In distribution
29367 In distribution
29171 In distribution
9196 In distribution
29187 In distribution
29181 In distribution
29186 In distribution
29503 In distribution
114 In distribution
119 In distribution
29140 In distribution
29470 In distribution
77000 In distribution
9041EL In distribution
9139 In distribution
29360 In distribution
29408 In distribution
9112 In distribution
9011 In distribution
9440 In distribution
9153N 5 In distribution
29182 In distribution
29360 In distribution
29180 In distribution
9114 In distribution
29475 In distribution
9197 In distribution
9106 In distribution
29189 In distribution
29475 In distribution
29137 In distribution
29121 In distribution
29158 In distribution
9194 In distribution
29365 In distribution
29186 In distribution
29137 In distribution
29118 In distribution
29153 In distribution
29367 In distribution
9185 In distribution
29170 In distribution
29136 In distribution
29146 In distribution
29163 In distribution
9274 In distribution
29470 In distribution
9103 In distribution
9165 In distribution
29604 In distribution
29140 In distribution
29170 In distribution
9100 In distribution
9185 In distribution
9183 In distribution
59180 In distribution
9571 In distribution
29276 In distribution
29245 In distribution
29160 In distribution
29153 In distribution
29120 In distribution
29160 In distribution
29121 In distribution
9131 In distribution
9114 In distribution
29146 In distribution
29480 In distribution
118CE Withdrawn
29107 Withdrawn
9131 Withdrawn
9109 Withdrawn
29158 Withdrawn
9183 Withdrawn
9040 Withdrawn
29480 Withdrawn
29171 Withdrawn
9112 Withdrawn
29470 Withdrawn
9183 Withdrawn
9010 Withdrawn
29490 Withdrawn
9041EL Withdrawn
32474 Withdrawn
29920 Withdrawn
9194 Withdrawn
9070 Withdrawn
29183 Withdrawn
9185 Withdrawn
29245 Withdrawn
29140 Withdrawn
9195 Withdrawn
29276 Withdrawn
9197 Withdrawn
29186 Withdrawn
9511 Withdrawn
9196 Withdrawn
9199 Withdrawn
9187 Withdrawn
29121 Withdrawn
9135 Withdrawn
29160 Withdrawn
9274 Withdrawn
59180 Withdrawn
29146 Withdrawn
9120 Withdrawn
9196 Withdrawn
9103 Withdrawn
29490 Withdrawn
29146 Withdrawn
9113 Withdrawn
9101 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Cardinal Health Cardinal Health 200, LLC 67,931
Medline Industries, Inc. Medline Industries, Inc. 54,362
Avid TruCustom Avid Medical, Inc. 13,498
Halyard Avid Medical, Inc. 12,802
ACS American Contract Systems, Inc. 10,337
SurgiTrack Owens & Minor Distribution, Inc. 5,575
Aligned Medical Solutions Aligned Medical Solutions 3,490
SurgiTrackSM Owens & Minor Distribution, Inc. 3,364
DeRoyal Deroyal Industries, Inc. 2,770
Medline Medline Industries, Inc. 1,960
Henry Schein Henry Schein, Inc. 729
Stradis Stradis Healthcare 685

Showing 12 of 113. All products under General Surgery Tray

Recalls Naming This Product

3 recalls name this product by its own identifiers, the UDI on its label.

Recalls naming the identifiers of Convertors
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Cardinal Health UDI-DI 2021-11-02 Class II Process control Potential for open packaging seals compromising the sterility of the surgical gowns 169,262 units
Cardinal Health UDI-DI 2021-11-02 Class II Process control Potential for open packaging seals compromising the sterility of the surgical gowns 231,219 units
Cardinal Health UDI-DI 2021-11-02 Class II Process control Potential for open packaging seals compromising the sterility of the surgical gowns 363,480 units

Recalls

9 of these are Class II. Class II means a temporary or reversible health consequence. 2 are recorded with the root cause “No Marketing Application”: the device was distributed without the premarket submission its class requires, a compliance finding rather than a defect. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2026-07-29 Class II Process change control The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These 846 units
2026-07-14 Class II Nonconforming Material/Component Cardinal Health was recently informed of a medical device recall from MEDICOM concerning the Ritmed Neurological Sponges. The recall is being issued due to unexpected variability of endotoxin levels on the products. 36862 kits
2024-11-08 Class II Material/Component Contamination Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits. 973,785 total units
2024-11-08 Class II Nonconforming Material/Component Potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits. 512,786 total units
2023-08-16 Class II Material/Component Contamination Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits). 13,351 total packs
2020-01-31 Class II Other The kits contained recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no assurance that the surgical gowns are sterile. An inadequately sterilized surgical gown 318,000 units 2023-02-01
2020-01-31 Class II Vendor change control The kits contained recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no assurance that the surgical gowns are sterile. An inadequately sterilized surgical go 2,161,526 units (113, 711 additional units as of 2/25/20) 2023-01-19
2018-11-16 Class II Unknown/Undetermined by firm The double wrapping of this custom kit basin set is not supported by the current sterility assurance validation. 182 packs 2019-11-04
2017-08-01 Class II Material/Component Contamination The firm manufactured and distributed Presource(R) kits which contained BD SafetyGlide” 22GA 1 inch Needles. BD subsequently recalled these needles because, ” Loose polypropylene particulate in the fluid path could be expelled out of the n 184,102 kits 2019-06-18
2012-01-27 Not classified Packaging change control The Presource kits were assembled with Ethicon Sutures in new Tyvek packaging which could no longer be placed in kits that will undergo ethylene oxide sterilization. 18,300 kits 2016-08-01
2011-12-23 Not classified No Marketing Application The Presource kits were assembled with a Jobri Infant Restraint Strap which does not have the appropriate 510(k) pre-market clearance. 15,369 kits in total 2016-08-01
2011-12-23 Not classified No Marketing Application The Presource kits were assembled with a Jobri Infant Restraint Strap which does not have the appropriate 510(k) pre-market clearance. 15,369 kits in total 2016-08-01
2011-12-12 Not classified PMA Some of the components contained in the Presource kits are being recalled because Cardinal Health has determined that the component manufacturer(s) does not have all necessary FDA registrations or filings needed for this product. 7,213 each 2016-08-29
2011-09-30 Not classified Component design/selection Some of the components contained in the Presource kits are being recalled because Cardinal Health has determined that the component manufacturers do not have all necessary FDA registrations or filings needed for these components. 2016-08-01
2011-09-03 Not classified Component design/selection Some of the components contained in the Presource kits are being recalled because Cardinal Health has determined that the component manufacturer(s) does not have all necessary FDA registrations or filings needed for this product. 2016-08-01
2011-01-28 Not classified Nonconforming Material/Component Esmark bandages placed in some Presource kits/modules may not have been adequately sterilized. 4.395 modules 2012-09-04
2006-09-27 Not classified Other The cardiovascular drape may tear and/or fray at the reinforced fenestrated trough area during use. 1,026 modules 2008-05-09
2006-09-27 Not classified Other The cardiovascular drape may tear and fray at the reinforced fenestrated trough area during use. 633 packs 2008-05-09
2006-09-27 Not classified Other The cardiovascular drape may tear and/or fray at the reinforced fenestrated trough area during use. 3,533 packs 2008-05-09
2005-10-03 Not classified Other The procedure kits labeled as latex-free may contain a 4′ or 6′ ultra-weave premium elastic bandage containing dry, natural rubber latex. 2006-12-21
2005-10-03 Not classified Other The procedure kits labeled as latex-free may contain a 4′ or 6′ ultra-weave premium elastic bandage containing dry, natural rubber latex. 2006-12-21
2003-06-27 Not classified Other The kits labeled as sterile were stolen in transit to the sterilizer and have not been sterilized. 2005-09-22
2003-06-27 Not classified Other The kits labeled as sterile were stolen in transit to the sterilizer and have not been sterilized. 2005-09-22
2003-06-27 Not classified Other The kits labeled as sterile were stolen in transit to the sterilizer and have not been sterilized. 2005-09-22
2003-06-27 Not classified Other The kits labeled as sterile were stolen in transit to the sterilizer and have not been sterilized. 2005-09-22
2003-06-27 Not classified Other The kits labeled as sterile were stolen in transit to the sterilizer and have not been sterilized. 1242 packs total – all five kits 2005-09-22

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer