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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
General-purpose surgical scissors, reusable FDA UDI
Device Name
STANDARD SCISSORS STRAIGHT FIG. 3 16,5CM FDA UDI
Model / Reference
8025-16. FDA UDI
Description
STANDARD SCISSORS STRAIGHT FIG. 3 16,5CM FDA UDI

Identifiers

Catalog Number
8025-16. FDA UDI
Primary DI / UDI-DI
04044684207344 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
General-purpose surgical scissors, 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: General-purpose surgical scissors, reusable

A standard hand-held manual surgical instrument designed to cut/dissect various tissues during open surgery, with no specific anatomy or clinical use. This device is available in various designs and sizes and can be made of metal or have carbide inserts.

Similar devices

Also classified as General-purpose surgical scissors, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9648fc04-6a6b-4c29-81a2-754d646cd7b8 35 fields · synced Oct 6, 2026