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Uni Femoral Knee

FDA UDI

Class II (US FDA UDI)

by Signal Medical Corp.

Identity

Trade Name
Uni Femoral Knee FDA UDI
Generic Name
Coated knee femur prosthesis FDA UDI
Device Name
Uni Femoral Knee Size 3 FDA UDI
Model / Reference
3 FDA UDI
Description
Uni Femoral Knee Size 3 FDA UDI

Identifiers

Catalog Number
WZ-1-1003 FDA UDI
Primary DI / UDI-DI
B046WZ110030 FDA UDI
510(k) Number
K012800 FDA UDI
FDA Product Code
HRY FDA UDI
GMDN Term
Coated knee femur prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3530 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Coated knee femur prosthesis

Uni Femoral Knee by Signal Medical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coated knee femur prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6a8769cd-619a-4f44-a7b4-36966d96bbfe 36 fields · synced May 30, 2026