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DemeGUT

FDA UDI

Class II (US FDA UDI)

by DemeTECH Corp

Identity

Trade Name
DemeGUT FDA UDI
Generic Name
Catgut suture, plain FDA UDI
Device Name
Plain Gut, Sterile, Absorbable Surgical Suture FDA UDI
Model / Reference
CP230048B16P FDA UDI
Description
Plain Gut, Sterile, Absorbable Surgical Suture FDA UDI

Identifiers

Primary DI / UDI-DI
10652927299981 FDA UDI
510(k) Number
K072930 FDA UDI
FDA Product Code
GAL FDA UDI
GMDN Term
Catgut suture, plain 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, plain

DemeGUT by DemeTECH Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Catgut suture, plain.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DemeTECH Corp

Sources (1)

  • FDA UDI a15c1d28-9e00-442d-913f-ec9642e9e585 36 fields · synced May 30, 2026