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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
Catgut suture, chromic FDA UDI
Device Name
SUTURE 3-0 Chromic Gut, 3-0 U.S.P. (3.0 Metric) 30"/76cm Absorbable Surgical Suture, DS18 Reverse Cutting 3/8 Circle 18 mm FDA UDI
Model / Reference
S636G FDA UDI
Description
SUTURE 3-0 Chromic Gut, 3-0 U.S.P. (3.0 Metric) 30"/76cm Absorbable Surgical Suture, DS18 Reverse Cutting 3/8 Circle 18 mm FDA UDI

Identifiers

Primary DI / UDI-DI
10612479189826 FDA UDI
FDA Product Code
GAL FDA UDI
GMDN Term
Catgut suture, chromic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4830 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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: Catgut suture, chromic

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

Similar devices

Also classified as Catgut suture, chromic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mckesson Medical-Surgical Inc.

Sources (1)

  • FDA UDI 9d204d22-767b-438a-b150-6fa7c8c4631b 33 fields · synced Jun 1, 2026