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Puragraft

FDA UDI

Class II (US FDA UDI)

by Surgical Specialties México, S. de R.L. de C.V.

Identity

Trade Name
Puragraft FDA UDI
Generic Name
Catgut suture, plain FDA UDI
Device Name
C6 3-0 Pl Gut 27"/70cm FDA UDI
Model / Reference
PGT554B FDA UDI
Description
C6 3-0 Pl Gut 27"/70cm FDA UDI

Identifiers

Primary DI / UDI-DI
00848782033133 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

Puragraft by Surgical Specialties México, S. de R.L. de C.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Catgut suture, plain.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 41656508-063f-4132-a07f-002bfadafe69 35 fields · synced May 30, 2026