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Patient Protective Pad

FDA UDI

Class I (US FDA UDI)

by Innovative Medical Products, Inc.

Identity

Trade Name
Patient Protective Pad FDA UDI
Generic Name
Surgical linen/cushion set FDA UDI
Device Name
Non-sterile Patient Protective Pad and Cohesive Wrap for De Mayo Knee Positioner® (25/case) FDA UDI
Model / Reference
294-NSP FDA UDI
Description
Non-sterile Patient Protective Pad and Cohesive Wrap for De Mayo Knee Positioner® (25/case) FDA UDI

Identifiers

Catalog Number
294-NSP FDA UDI
Primary DI / UDI-DI
00696588002330 FDA UDI
FDA Product Code
FMP FDA UDI
GMDN Term
Surgical linen/cushion set 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

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical linen/cushion set

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

Similar devices

Also classified as Surgical linen/cushion set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e5f7e31c-1982-4a36-bfa5-e7b535e77c45 34 fields · synced Jun 8, 2026