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Instrument

FDA UDI

Class I (US FDA UDI)

by Howmedica Osteonics Corp.

Identity

Trade Name
INSTRUMENT FDA UDI
Generic Name
Orthopaedic bone pin, non-bioabsorbable FDA UDI
Device Name
DISPOSABLE FLUTED HEADLESS PINS FDA UDI
Model / Reference
7650-2038A FDA UDI
Description
DISPOSABLE FLUTED HEADLESS PINS FDA UDI

Identifiers

Catalog Number
7650-2038A FDA UDI
Primary DI / UDI-DI
07613327255959 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic bone pin, non-bioabsorbable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 89.0 Millimeter FDA UDI

Category: Orthopaedic bone pin, non-bioabsorbable

Instrument by Howmedica Osteonics Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone pin, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 82381dd0-4682-4204-afde-dfedffe7f9dd 35 fields · synced Jun 1, 2026