← Back to catalogue

Suture Cutter

FDA UDI

Class I (US FDA UDI)

by T.a.g Medical Products Agricultural Cooperative Association

Identity

Trade Name
Suture Cutter FDA UDI
Generic Name
Suture cutter, reusable FDA UDI
Model / Reference
B FDA UDI

Identifiers

Catalog Number
231400t FDA UDI
Primary DI / UDI-DI
10810190016821 FDA UDI
FDA Product Code
HXZ FDA UDI
GMDN Term
Suture cutter, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Suture cutter, reusable

Suture Cutter by T.a.g Medical Products Agricultural Cooperative Association — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suture cutter, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
T.a.g Medical Products Agricultural Cooperative Association

Sources (1)

  • FDA UDI 38c9c8ef-a904-493c-8738-ac53e7976cf1 33 fields · synced May 30, 2026