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McKesson

FDA UDI

Class II (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
McKesson FDA UDI
Generic Name
Polyglycolic acid suture FDA UDI
Device Name
SUTURE 4-0 Polyglycolic Acid, Undyed, Braided, Coated 4-0 U.S.P. (1.5 Metric) 18"/46cm Synthetic Absorbable Surgical Suture, PC31 Precision Reverse Cutting 3/8 Circle 18 mm FDA UDI
Model / Reference
SJ496G FDA UDI
Description
SUTURE 4-0 Polyglycolic Acid, Undyed, Braided, Coated 4-0 U.S.P. (1.5 Metric) 18"/46cm Synthetic Absorbable Surgical Suture, PC31 Precision Reverse Cutting 3/8 Circle 18 mm FDA UDI

Identifiers

Primary DI / UDI-DI
10612479189604 FDA UDI
FDA Product Code
GAM FDA UDI
GMDN Term
Polyglycolic acid suture FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4493 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Polyglycolic acid suture

McKesson by Mckesson Medical-Surgical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyglycolic acid suture.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dce890e6-30f3-40f7-91bd-0a1a5d300932 33 fields · synced Jun 1, 2026