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Telegraph®

FDA UDI

Class II (US FDA UDI)

by Fournitures Hospitalieres Industrie

Identity

Trade Name
TELEGRAPH® FDA UDI
Generic Name
Humerus intramedullary nail FDA UDI
Model / Reference
250845 - LONG HUMERAL NAIL, Ø10/L270, TITANIUM FDA UDI

Identifiers

Primary DI / UDI-DI
03661489508455 FDA UDI
510(k) Number
K042332 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: Humerus intramedullary nail

Telegraph® by Fournitures Hospitalieres Industrie — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Humerus intramedullary nail.

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 f395ae1a-a5b8-4bc4-965d-9defb77f1dc7 33 fields · synced Jun 1, 2026