← Back to catalogue

OrthoMedFlex

FDA UDI

Class II (US FDA UDI)

by Orthomedflex Llc

Identity

Trade Name
OrthoMedFlex FDA UDI
Generic Name
Ceramic femoral head prosthesis FDA UDI
Device Name
Ceramic Femoral Head, 36mm, S (-4.0 mm) FDA UDI
Model / Reference
AH3-136 FDA UDI
Description
Ceramic Femoral Head, 36mm, S (-4.0 mm) FDA UDI

Identifiers

Catalog Number
AH3-136 FDA UDI
Primary DI / UDI-DI
M716AH31360 FDA UDI
FDA Product Code
LZO FDA UDI
GMDN Term
Ceramic femoral head prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 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: Ceramic femoral head prosthesis

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

Similar devices

Also classified as Ceramic femoral head prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Orthomedflex Llc

Sources (1)

  • FDA UDI a416bbd6-5dcb-43f5-9001-a442d24c8182 35 fields · synced May 30, 2026