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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
Humeral head prosthesis trial, reusable FDA UDI
Model / Reference
79652815 FDA UDI

Identifiers

Primary DI / UDI-DI
04048844293444 FDA UDI
FDA Product Code
KWY FDA UDI
GMDN Term
Humeral head prosthesis trial, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3390 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: Humeral head prosthesis trial, reusable

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 Humeral head prosthesis trial, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
implantcast GmbH

Sources (1)

  • FDA UDI c5e4866b-d315-4d6d-bb44-7a711a40da50 33 fields · synced May 30, 2026