← Back to catalogue

OrthoMedFlex

FDA UDI

Class II (US FDA UDI)

by Orthomedflex Llc

Identity

Trade Name
OrthoMedFlex FDA UDI
Generic Name
Acetabulum prosthesis hole plug FDA UDI
Device Name
Tryon Apical Screw, SIZE 7/16 UNF, TiAI4V Alloy with Anodising FDA UDI
Model / Reference
AHC-1 FDA UDI
Description
Tryon Apical Screw, SIZE 7/16 UNF, TiAI4V Alloy with Anodising FDA UDI

Identifiers

Catalog Number
AHC-1 FDA UDI
Primary DI / UDI-DI
M716AHC10 FDA UDI
FDA Product Code
LPH FDA UDI
GMDN Term
Acetabulum prosthesis hole plug 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: Acetabulum prosthesis hole plug

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

Similar devices

Also classified as Acetabulum prosthesis hole plug.

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 58c9776a-7304-4964-b40f-883533b673d9 35 fields · synced Jun 8, 2026