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Tri-Lobe Adapter

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 239-0015

by Tecomet, Inc

Identity

Trade Name
Tri-Lobe Adapter EUDAMED
Tecomet FDA UDI
Generic Name
Orthopaedic implant-instrument extension adaptor, reusable FDA UDI
Device Name
Extensions EUDAMED
Tri-Lobe Adaptor FDA UDI
Model / Reference
239-0015 EUDAMEDFDA UDI
Description
Tri-Lobe Adaptor FDA UDI

Identifiers

Primary DI / UDI-DI
00841435102743 EUDAMEDFDA UDI
Basic UDI-DI
0841435147847VQ EUDAMED
Direct Marketing DI
00841435102743 EUDAMED
FDA Product Code
HTW FDA UDI
EMDN Code
L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Orthopaedic implant-instrument extension adaptor, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 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

Tri-Lobe Adapter 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 8a35beff-624c-4253-aba0-f2a2a3e6fc19 61 fields · synced Sep 18, 2026
  • FDA UDI e7575f57-f353-441f-8f4d-0700e1d65e10 33 fields · synced May 30, 2026