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Amf Revision Tt Cones

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
AMF REVISION TT CONES FDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Device Name
AMF Revision TT Cones - Femur Alignment Rod FDA UDI
Model / Reference
906C.10.950 FDA UDI
Description
AMF Revision TT Cones - Femur Alignment Rod FDA UDI

Identifiers

Catalog Number
906C.10.950 FDA UDI
Primary DI / UDI-DI
08033390191173 FDA UDI
FDA Product Code
JWH FDA UDI
MBH FDA UDI
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 FDA UDI
888.3565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic prosthesis implantation positioning instrument, reusable

Amf Revision Tt Cones by Limacorporate — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic prosthesis implantation positioning instrument, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI d07ca723-6142-4684-a363-d0931377c5cf 34 fields · synced May 31, 2026