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TELEGRAPH® EVOLUTION Humeral Nailing System

FDA UDI

Class II (US FDA UDI)

by Fournitures Hospitalieres Industrie

Identity

Trade Name
TELEGRAPH® EVOLUTION Humeral Nailing System FDA UDI
Generic Name
Humerus intramedullary nail FDA UDI
Model / Reference
270759 - TELEGRAPH EVOLUTION CANNULATED HUMERAL NAIL LONG LEFT D9 L210 FDA UDI

Identifiers

Primary DI / UDI-DI
03661489707599 FDA UDI
510(k) Number
K200127 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Humerus intramedullary nail FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthopaedic bone screw, non-bioabsorbable, sterileHumerus intramedullary nailOrthopaedic bone washer, sterile

TELEGRAPH® EVOLUTION Humeral Nailing System by Fournitures Hospitalieres Industrie — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone washer, sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c9243021-5777-4fcb-9f06-203d98102514 33 fields · synced Jun 1, 2026