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Tekno®

FDA UDI

Class I (US FDA UDI)

by Tekno Medical Optik-Chirurgie GmbH & Co.

Identity

Trade Name
TEKNO® FDA UDI
Generic Name
Dressing/utility forceps, tweezers-like, reusable FDA UDI
Device Name
ADSON TISSUE FORCEPS 12CM 1X2 TEETH FDA UDI
Model / Reference
11200-12 FDA UDI
Description
ADSON TISSUE FORCEPS 12CM 1X2 TEETH FDA UDI

Identifiers

Catalog Number
11200-12 FDA UDI
Primary DI / UDI-DI
04044684011781 FDA UDI
FDA Product Code
GEN FDA UDI
GMDN Term
Dressing/utility forceps, tweezers-like, reusable 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dressing/utility forceps, tweezers-like, reusable

Tekno® by Tekno Medical Optik-Chirurgie GmbH & Co. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dressing/utility forceps, tweezers-like, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tekno Medical Optik-Chirurgie GmbH & Co.

Sources (1)

  • FDA UDI e3786411-a246-49c4-a7e2-20072a573927 35 fields · synced Jun 8, 2026