Henry Schein

HS PC31 5-0 BK MN NYL 18"/45CM

Registry build 21.09.26
3manufacturers in China registered for this device type
26catalogue numbers in this listing

Who Else Makes It

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

Chinese manufacturers registered for FDA product code GAR
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 Henry Schein
Listed by Henry Schein, Inc., United States
FDA product code GAR
Device type Suture, Nonabsorbable, Synthetic, Polyamide
Device class Class 2
Regulation 21 CFR 878.5020
Record published 2018-05-08
Record revised 2024-11-07 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Ethylene Oxide
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Storage Special storage condition: N/A
Packaging Pack of 12
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Henry Schein
Catalogue number Size Per pack Status
570-1044 36 In distribution
101-1209 In distribution
570-1040 12 In distribution
101-7137 In distribution
570-1050 12 In distribution
900-7466 In distribution
900-7482 In distribution
5700479 3-0 USP In distribution
570-1039 12 In distribution
5700480 3-0 USP In distribution
101-6053 In distribution
900-7460 In distribution
570-1398 12 In distribution
5700458 5-0 USP In distribution
900-7470 In distribution
900-7476 In distribution
900-7461 In distribution
900-7459 In distribution
900-7472 In distribution
900-7473 In distribution
570-1043 12 In distribution
900-7464 In distribution
570-1042 12 In distribution
900-7487 In distribution
101-3728 In distribution
5700459 4-0 USP In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DemeLON Demetech Corp. 1,800
Dafilon B Braun Surgical SA 592
WEGO-Nylon Non-absorbable Surgical Suture With Needle Foosin Medical Supplies Inc.ltd 279
Ethilon Ethicon, Inc. 272
Monosof Covidien LP 256
DemeLON Multi Demetech Corp. 227
Surgilon Covidien LP 135
Atramat Internacional Farmacéutica S.A DE C.V 127
Supramid Extra S. Jackson, Inc. 119
Mani Sutures Nylon Mani, Inc. 88
Onatec Surgical Specialties México, S. de R.L. de C.V. 75
Sharpoint Plus Surgical Specialties México, S. de R.L. de C.V. 73

Showing 12 of 284. All products under Suture, Nonabsorbable, Synthetic, Polyamide

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
N85060 1988-02-22 NONABSORBABLE SURG. SUTURES, NYLON Deknatel, Inc.
N85316 1986-06-20 ETHILON/NUROLON NYLON SUTURES Ethicon, Inc.
N80838 1985-07-23 SUPRAMID EXTRA SUTURES S. Jackson, Inc.
N83511 1982-05-18 NON-ABSORBABLE SUTURES NYLON Davis & Geck, 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