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Columbus® CR/PS

FDA UDI

Class II (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
Columbus® CR/PS FDA UDI
Generic Name
Coated knee tibia prosthesis FDA UDI
Device Name
COLUMBUS CR/PS TIB.PLAT.PLASMAPORE T2 FDA UDI
Model / Reference
NN083K FDA UDI
Description
COLUMBUS CR/PS TIB.PLAT.PLASMAPORE T2 FDA UDI

Identifiers

Catalog Number
NN083K FDA UDI
Primary DI / UDI-DI
04038653351817 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Coated knee tibia prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 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: Coated knee tibia prosthesis

Columbus® CR/PS by Aesculap, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coated knee tibia prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI 473c2590-7be3-4c79-a96e-b6f49564ee99 36 fields · synced May 30, 2026