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Tecomet

FDA UDI

Class I (US FDA UDI)

by Tecomet, Inc

Identity

Trade Name
Tecomet FDA UDI
Generic Name
Surgical flat-nosed pliers FDA UDI
Device Name
Extraction Pliers FDA UDI
Model / Reference
46572 FDA UDI
Description
Extraction Pliers FDA UDI

Identifiers

Primary DI / UDI-DI
00841435111080 FDA UDI
FDA Product Code
HTC FDA UDI
GMDN Term
Surgical flat-nosed pliers FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Surgical flat-nosed pliers

Tecomet Extraction Pliers are a high-quality, heavy-duty surgical instrument designed for general surgery applications. Featuring sturdy handles and gripping jaws, these pliers provide exceptional grip and leverage during complex procedures.

Similar devices

Also classified as Surgical flat-nosed pliers.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tecomet, Inc

Sources (1)

  • FDA UDI 0980a40e-ff25-4d8e-8833-044936eaabd2 33 fields · synced Sep 18, 2026