← Back to catalogue

Telegraph Evo Couvercle

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 270805

by Fournitures Hospitalieres Industrie

Identity

Trade Name
TELEGRAPH EVO COUVERCLE EUDAMED
TELEGRAPH® EVOLUTION Humeral Nailing System FDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Device Name
TRAYS, LIDS, MATS EUDAMED
Model / Reference
270805 EUDAMED
270805- TELEGRAPH EVOLUTION LID FDA UDI

Identifiers

Primary DI / UDI-DI
03661489708053 EUDAMEDFDA UDI
Basic UDI-DI
3661489PANIERCIAH EUDAMED
Direct Marketing DI
03661489708053 EUDAMED
510(k) Number
K200127 FDA UDI
FDA Product Code
HSB FDA UDI
EMDN Code
V0499 CLINICAL USE CONTAINERS (NON-IVD) - OTHER EUDAMED
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

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

No

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

No

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

Category: Instrument transport trolley system

Telegraph Evo Couvercle by Fournitures Hospitalieres Industrie — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument transport trolley system.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
FR-MF-000000819

Sources (2)

  • EUDAMED 778eebab-3950-4afc-89f3-ef936679a444 61 fields · synced Jun 19, 2026
  • FDA UDI 0440cfa3-f945-47c6-8602-04f485a5cbfa 33 fields · synced May 30, 2026