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Coflex Tlc Lite

EUDAMED

Class I (EU MDR)

Ref 7802TN-022Model COFLEX TLC LITE

by Andover Healthcare Inc.

Identity

Trade Name
COFLEX TLC LITE EUDAMED
Device Name
COFLEX TLC EUDAMED
Model / Reference
COFLEX TLC LITE EUDAMED
7802TN-022 EUDAMED

Identifiers

Primary DI / UDI-DI
00724004621671 EUDAMED
Basic UDI-DI
0724004CoFlexTLCLITEXL EUDAMED
EMDN Code
M03040299 ELASTIC SUPPORT BANDAGES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Denmark EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

Yes

EUDAMED

Coflex Tlc Lite by Andover Healthcare Inc. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
US-MF-000035055
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED 7e0a4347-6d94-4471-b178-36e9dca4ed24 61 fields · synced Oct 7, 2026