Fssb

2xHRS-13.0-300 USP 5-0 Polypropylene blue 75 cm Pledget 3x3. sterile VA9.8

Registry build 21.09.26
3manufacturers in China registered for this device type
58catalogue numbers in this listing

Who Else Makes It

Concentrated in Shandong (2), Beijing (1).

Chinese manufacturers registered for FDA product code GAW
Manufacturer City Province Registered as Device types
Shandong Haidike Medical Products Co., Ltd. Heze Shandong Manufacturer 22
Foosin Medical Supplies Inc.ltd Weihai Shandong Manufacturer 8
ARC Medical Supplies (Beijing) Co., Ltd. Beijing Beijing Manufacturer 7

Record

Regulatory record for Fssb
Listed by Surgical Specialties México, S. de R.L. de C.V.
FDA product code GAW
Device type Suture, Nonabsorbable, Synthetic, Polypropylene
Device class Class 2
Regulation 21 CFR 878.5010
Record published 2021-10-22
Record revised 2024-11-11 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Box of 12, box of 36, box of 24
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Fssb
Catalogue number Size Status
E012PP3 8-0 USP In distribution
E112PP 5-0 USP In distribution
E251PP 8-0 USP In distribution
H002PP3 8-0 USP In distribution
E064PP 4-0 USP In distribution
H001PP3 8-0 USP In distribution
H062PP 6-0 USP In distribution
E112PP2 5-0 USP In distribution
A029PP 10-0 USP In distribution
A048PP 30 cm In distribution
E256PP 3-0 USP In distribution
E033PP3 8-0 USP In distribution
A052PP 10 cm In distribution
A011PP 30 cm In distribution
A062PP 9-0 USP In distribution
E033PP 8-0 USP In distribution
E252PP 7-0 USP In distribution
A030PP 100 usp In distribution
A022PP 10-0 USP In distribution
E062PP 3-0 USP In distribution
E136PP3 6-0 USP In distribution
E257PP 3-0 USP In distribution
E047PP 7-0 USP In distribution
A046PP 10-0 USP In distribution
H025PP 7-0 USP In distribution
A003PP 10-0 USP In distribution
E068PP 3-0 USP In distribution
E258PP 4-0 USP In distribution
G012PP 6-0 USP In distribution
A055PP 10-0 USP In distribution
E044PP 6-0 USP In distribution
E253PP 7-0 USP In distribution
E081PP 5-0 USP In distribution
A028PP 23 cm In distribution
E046PP 8-0 USP In distribution
D034PP 45 cm In distribution
E067PP 4-0 USP In distribution
E065PP 3-0 USP In distribution
E061PP 4-0 USP In distribution
E060PP 5-0 USP In distribution
E151PP 4-0 USP In distribution
A039PP 10-0 USP In distribution
E148PP 7-0 USP In distribution
D033PP 45 cm In distribution
E048PP 6-0 USP In distribution
H001PP 45 cm In distribution
H008PP 5-0 USP In distribution
A058PP 6-0 USP In distribution
A033PP 100 usp In distribution
A073PP 10-0 USP In distribution
E029PP 5-0 USP In distribution
A049PP 30 cm In distribution
H006PP 6-0 USP In distribution
A018PP 10-0 USP In distribution
H002PP 60 cm In distribution
A001PP 10-0 USP In distribution
E190PP 5-0 USP In distribution
D036PP 6-0 USP In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DemeLENE Demetech Corp. 1,707
Premilene B Braun Surgical SA 1,247
Optilene B Braun Surgical SA 1,110
Prolene Ethicon, Inc. 765
Deknatel Teleflex Medical LLC 373
Corolene® Peters Surgical 354
WEGO-Polypropylene Nonabsorbable Surgical Suture With Needle Foosin Medical Supplies Inc.ltd 346
Surgipro II Covidien LP 254
Surgipro ll Covidien LP 152
Atramat Internacional Farmacéutica S.A DE C.V 140
Surgipro Covidien LP 133
Filaprop Meril Endo Surgery PVT. Ltd. 123

Showing 12 of 200. All products under Suture, Nonabsorbable, Synthetic, Polypropylene

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P890002 1989-05-31 POLYPROPYLENE SURGICAL SUTURE Alcon Laboratories, Inc.
P820083 1986-08-05 GORE-TEX(R) EXPANDED PTFE SUTURE W. L. Gore & Associates, Inc.

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