← Back to catalogue

plug

FDA UDI

Class II (US FDA UDI)

by implantcast GmbH

Identity

Trade Name
plug FDA UDI
Generic Name
Acetabulum prosthesis hole plug FDA UDI
Model / Reference
02200001 FDA UDI

Identifiers

Primary DI / UDI-DI
04048844108533 FDA UDI
FDA Product Code
LZO FDA UDI
GMDN Term
Acetabulum prosthesis hole plug 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Acetabulum prosthesis hole plug

plug by implantcast GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Acetabulum prosthesis hole plug.

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
implantcast GmbH

Sources (1)

  • FDA UDI f7cc1912-5ee7-4f1c-9d11-a39d47720f5f 32 fields · synced Jun 8, 2026