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Suture Manipulator Grasper

FDA UDI

Class I (US FDA UDI)

by T.a.g Medical Products Agricultural Cooperative Association

Identity

Trade Name
Suture Manipulator Grasper FDA UDI
Generic Name
Clamp manipulation forceps FDA UDI
Model / Reference
601200p FDA UDI

Identifiers

Catalog Number
601200p FDA UDI
Primary DI / UDI-DI
10818674025963 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Clamp manipulation forceps 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Suturing unit, reusableClamp manipulation forceps

Suture Manipulator Grasper by T.a.g Medical Products Agricultural Cooperative Association — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Clamp manipulation forceps.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f75377ed-a6c2-47e3-889c-a0a30ec4e7b2 33 fields · synced May 29, 2026