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OrthoMedFlex

FDA UDI

Class II (US FDA UDI)

by Orthomedflex Llc

Identity

Trade Name
OrthoMedFlex FDA UDI
Generic Name
Metallic femoral head prosthesis FDA UDI
Device Name
Femoral Head, SIZE 28mm, (L) CoCr Alloy FDA UDI
Model / Reference
AH1-328 FDA UDI
Description
Femoral Head, SIZE 28mm, (L) CoCr Alloy FDA UDI

Identifiers

Catalog Number
AH1-328 FDA UDI
Primary DI / UDI-DI
M716AH13280 FDA UDI
FDA Product Code
LPH FDA UDI
GMDN Term
Metallic femoral head prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Metallic femoral head prosthesis

OrthoMedFlex by Orthomedflex Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic femoral head prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Orthomedflex Llc

Sources (1)

  • FDA UDI 4cedb8fd-f3d0-4677-9642-53824aeb9eaa 35 fields · synced May 30, 2026