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Chromic Gut

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Chromic Gut FDA UDI
Generic Name
Catgut suture, chromic FDA UDI
Device Name
Absorbable Suture FDA UDI
Model / Reference
CG-415 FDA UDI
Description
Absorbable Suture FDA UDI

Identifiers

Primary DI / UDI-DI
10884521053632 FDA UDI
510(k) Number
K142656 FDA UDI
K885018 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

Dimensions & Sizes

Size
Length — 30 Inch FDA UDI

Category: Catgut suture, chromic

Chromic Gut by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Catgut suture, chromic.

Cleared under the same submission

K142656 also covers:

K885018 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI 8bfd3f96-5660-43d2-822e-378a6bf3fa8c 37 fields · synced Jun 8, 2026