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TELEGRAPH® EVOLUTION Humeral Nailing System

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 270811

by Fournitures Hospitalieres Industrie

Identity

Trade Name
TELEGRAPH EVO CANNULATED REAMER D10 EUDAMED
TELEGRAPH® EVOLUTION Humeral Nailing System FDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Device Name
TELEGRAPH EVOLUTION reusable instruments EUDAMED
Model / Reference
270811 EUDAMED
270811 - TELEGRAPH EVOLUTION CANNULATED REAMER D10 FDA UDI

Identifiers

Primary DI / UDI-DI
03661489708114 EUDAMEDFDA UDI
Basic UDI-DI
3661489TELEVOCIRMM3 EUDAMED
Direct Marketing DI
03661489708114 EUDAMED
510(k) Number
K200127 FDA UDI
FDA Product Code
HSB FDA UDI
EMDN Code
L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - 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

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

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: Orthopaedic prosthesis implantation positioning instrument, reusable

TELEGRAPH® EVOLUTION Humeral Nailing System by Fournitures Hospitalieres Industrie — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED

Similar devices

Also classified as Orthopaedic prosthesis implantation positioning instrument, reusable.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 1f0c9bd4-f265-436c-b7c6-99f3d63febb0 33 fields · synced Oct 5, 2026
  • EUDAMED cdad4f9f-48b5-4602-ba81-45d3747d6ad6 61 fields · synced Oct 5, 2026