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OrthoMedFlex

FDA UDI

Class II (US FDA UDI)

by Orthomedflex Llc

Identity

Trade Name
OrthoMedFlex FDA UDI
Generic Name
Press-fit femoral stem prosthesis FDA UDI
Device Name
Kratos Hip Stem, SIZE 16 Lateral Offset, Ti6AI4V Alloy with HA Coating FDA UDI
Model / Reference
AS-216 FDA UDI
Description
Kratos Hip Stem, SIZE 16 Lateral Offset, Ti6AI4V Alloy with HA Coating FDA UDI

Identifiers

Catalog Number
AS-216 FDA UDI
Primary DI / UDI-DI
M716AS2160 FDA UDI
FDA Product Code
MEH FDA UDI
GMDN Term
Press-fit femoral stem 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: Press-fit femoral stem prosthesis

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

Similar devices

Also classified as Press-fit femoral stem 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 8b257c5d-d561-4776-883f-119c11adbb55 35 fields · synced May 29, 2026