← Back to catalogue

Amf Revision Tt Cones

FDA UDI

Class I (US FDA UDI)

by Limacorporate

Identity

Trade Name
AMF REVISION TT CONES FDA UDI
Generic Name
Surgical implant template, reusable FDA UDI
Device Name
AMF Revision TT Cones - Central Tibia Phantom Dia. 27 mm FDA UDI
Model / Reference
906C.21.027 FDA UDI
Description
AMF Revision TT Cones - Central Tibia Phantom Dia. 27 mm FDA UDI

Identifiers

Catalog Number
906C.21.027 FDA UDI
Primary DI / UDI-DI
08033390185950 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Surgical implant template, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

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: Surgical implant template, reusable

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

Similar devices

Also classified as Surgical implant template, reusable.

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
Limacorporate

Sources (1)

  • FDA UDI 7197cbe1-797a-438f-a508-289b200b941c 35 fields · synced Jun 6, 2026