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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
Dental dressing forceps, reusable FDA UDI
Device Name
LONDON-COLLEGE TWEEZERS 15 CM FIG. 5 FDA UDI
Model / Reference
70064-05 FDA UDI
Description
LONDON-COLLEGE TWEEZERS 15 CM FIG. 5 FDA UDI

Identifiers

Catalog Number
70064-05 FDA UDI
Primary DI / UDI-DI
04044684075608 FDA UDI
FDA Product Code
EFL FDA UDI
GMDN Term
Dental dressing forceps, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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: Dental dressing forceps, 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 Dental dressing forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f196eec8-8b52-4f93-be3c-8a4ca49e4711 35 fields · synced May 30, 2026