Medline

Suture Removal Tray 3.5' Litt Scissors

Registry build 21.09.26
12manufacturers in China registered for this device type
42catalogue numbers in this listing

Who Else Makes It

Concentrated in Jiangsu (6), Zhejiang (2), Hubei (2). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MCZ
Manufacturer City Province Registered as Device types
Conod Medical Co., Limited Changshu Jiangsu Contract manufacturer 48
Allmed Medical Products Co., Ltd. Zhijiang Hubei Contract manufacturer 43
Primecare Medical (Suzhou) Co., Ltd. Changshu Jiangsu Contract manufacturer 20
Derma Sciences Nantong Incorporation Development Jiangsu Contract manufacturer 19
Jiangsu Classic NEW-Type Medical Products Co., Ltd. Yancheng Jiangsu Contract manufacturer 13
Jiangsu NEW Pentastar Medical Products Co., Ltd. Changzhou Jiangsu Exporter 146
Zhejiang Lidesen Medical Instrument Co., Ltd. Hangzhou Zhejiang Contract manufacturer 100
Amsino Medical (Kunshan) Co., Ltd. Kunshan Jiangsu Contract manufacturer 53
Allmed Industrial Limited Shenzhen Guangdong Manufacturer 42
Hubei Lanbin Medical Group Co., Ltd. Xiaogan Hubei Contract manufacturer 33
Hangzhou Primecare Medical Co., Ltd. Hangzhou Zhejiang Contract manufacturer 29
Excellent Medical Technology Co., Ltd. Hong Kong Hong Kong Specification developer 17

Record

Regulatory record for Medline
Listed by Medline Industries, Inc., United States
FDA product code MCZ
Device type Suture Removal Kit
Device class Class 1
Regulation 21 CFR 878.4800
Premarket notification Exempt
Record published 2021-10-11
Record revised 2022-11-28 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Packaging Case of 50, case of 24, case of 20
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Medline
Catalogue number Size Status
60425 In distribution
60325 In distribution
SR60600 In distribution
55645 In distribution
55335 In distribution
55585 In distribution
57110 In distribution
TRI55165 In distribution
55395 In distribution
55525 In distribution
55295 In distribution
59865 In distribution
55410 In distribution
TRI44100 In distribution
60125 In distribution
DYNDR1142 In distribution
55200 In distribution
56100 In distribution
55645 In distribution
60215 In distribution
55615 In distribution
60465 In distribution
DYNDR1269 In distribution
DYNDR1273 In distribution
55200 In distribution
DYNDR1105A In distribution
SR60710 In distribution
55150 In distribution
SR510 In distribution
55650 In distribution
86125 In distribution
TRI55405 In distribution
SR60585 In distribution
55270 In distribution
SR60555 In distribution
60360 In distribution
55300 In distribution
54920 In distribution
DYNDR1248 In distribution
TRI44105 In distribution
TRI55115 In distribution
60280 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Cardinal Health Cardinal Health 200, LLC 166
Medical Action Industries Medical Action Industries, Inc. 99
Centurion Centurion Medical Products Corporation 71
Medline Industries, Inc. Medline Industries, Inc. 48
LSL Healthcare Lsl Industries, Inc. 42
E.M Adams Co., Inc. E.M. Adams Co., Inc. 33
Novaplus® Medical Action Industries, Inc. 16
McKesson Mckesson Medical-Surgical Inc. 11
Trinity Sterile, Inc. Trinity Sterile, Inc. 10
Stradis Healthcare Stradis Healthcare 8
Centurion Medical Products Corp Medline Industries, Inc. 8
MediChoice Owens & Minor Distribution, Inc. 8

Showing 12 of 35. All products under Suture Removal Kit

Recalls Naming This Product

1 recall names this product by its own identifier, the UDI on its label.

Recalls naming the identifiers of Medline
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Medline Industries, LP – Northfield UDI-DI 2024-02-23 Class II Process control Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users. 23,290 units

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