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Patient Protective Pad for Knee Postioners - CASE

FDA UDI

Class I (US FDA UDI)

by Innovative Medical Products, Inc.

Identity

Trade Name
Patient Protective Pad for Knee Postioners - CASE FDA UDI
Generic Name
Orthopaedic knee/leg holder liner FDA UDI
Device Name
Patient Protective Pad for Knee Positioners - CASE FDA UDI
Model / Reference
M-408-10 Stryker 110550 FDA UDI
Description
Patient Protective Pad for Knee Positioners - CASE FDA UDI

Identifiers

Catalog Number
M-408-10 Stryker 110550 FDA UDI
Primary DI / UDI-DI
30696588000917 FDA UDI
FDA Product Code
FMP FDA UDI
GMDN Term
Orthopaedic knee/leg holder liner FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6450 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthopaedic knee/leg holder liner

Patient Protective Pad for Knee Postioners - CASE by Innovative Medical Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic knee/leg holder liner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2cfcd106-3d0e-4707-a12f-8e4a8be6f6d7 34 fields · synced May 30, 2026