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Hi-Level Bandage Scissors

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 2768-00-000

by Tecomet, Inc

Identity

Trade Name
HI-LEVEL BANDAGE SCISSORS EUDAMED
Tecomet FDA UDI
Generic Name
General-purpose surgical scissors, reusable FDA UDI
Device Name
Scissors and Shears EUDAMED
HI-LEVEL BANDAGE SCISSORS FDA UDI
Model / Reference
2768-00-000 EUDAMEDFDA UDI
Description
HI-LEVEL BANDAGE SCISSORS FDA UDI

Identifiers

Primary DI / UDI-DI
00841435121577 EUDAMEDFDA UDI
Basic UDI-DI
0841435138727V9 EUDAMED
Direct Marketing DI
00841435121577 EUDAMED
FDA Product Code
LRW FDA UDI
EMDN Code
L01041299 ORTHOPAEDIC SURGERY SCISSORS, REUSABLE - OTHER EUDAMED
GMDN Term
General-purpose surgical scissors, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Hi-Level Bandage Scissors by Tecomet, Inc — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tecomet, Inc
EUDAMED SRN
US-MF-000027544
Authorised Representative
Meditec Source GmbH & Co. KG DE-AR-000009318

Sources (2)

  • EUDAMED a649707b-5a21-4bf3-89ed-de29bbd9de4c 61 fields · synced Sep 18, 2026
  • FDA UDI d01efdd6-5539-4026-aac2-b3f4c4098d78 33 fields · synced May 29, 2026