Amf Revision Tt Cones

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name: AMF REVISION TT CONES FDA UDI
Generic Name: Sleeve femoral/tibial extension, coated FDA UDI
Device Name: AMF Revision TT Cones - TT REV CONE Bicondylar Femur Dia. 24 mm - Right FDA UDI
Model / Reference: 6C12.14.R24 FDA UDI
Description: AMF Revision TT Cones - TT REV CONE Bicondylar Femur Dia. 24 mm - Right FDA UDI

Identifiers

Catalog Number: 6C12.14.R24 FDA UDI
Primary DI / UDI-DI: 08033390180832 FDA UDI
FDA Product Code: JWH FDA UDI
MBH FDA UDI
GMDN Term: Sleeve femoral/tibial extension, coated 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Sleeve femoral/tibial extension, coated

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

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Also classified as Sleeve femoral/tibial extension, coated.

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Coated Revision Stem — Signal Medical Corp. · Class II
S-ROM ZTT — DEPUY ORTHOPAEDICS, INC. · Class III
Coated Revision Stem — Signal Medical Corp. · Class II
ATTUNE — DEPUY (IRELAND) · Class III

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Limacorporate

Sources (1)

FDA UDI 904cf915-7123-4dca-b021-a384e96b2018 35 fields · synced Jun 1, 2026