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trial head taper 12/14mm

FDA UDI

Class II (US FDA UDI)

by implantcast GmbH

Identity

Trade Name
trial head taper 12/14mm FDA UDI
Generic Name
General internal orthopaedic fixation system implantation kit FDA UDI
Model / Reference
79653210 FDA UDI

Identifiers

Primary DI / UDI-DI
04048844293499 FDA UDI
FDA Product Code
LZO FDA UDI
GMDN Term
General internal orthopaedic fixation system implantation kit 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

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: General internal orthopaedic fixation system implantation kit

trial head taper 12/14mm by implantcast GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General internal orthopaedic fixation system implantation kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
implantcast GmbH

Sources (1)

  • FDA UDI 1bf1e29d-f8ae-42d3-8a81-c26f99dd10ad 33 fields · synced May 30, 2026