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PPS Glide

FDA UDI

Class II (US FDA UDI)

by Patient Positioning Systems, Llc

Identity

Trade Name
PPS Glide FDA UDI
Generic Name
Inflatable patient transfer sliding mattress, reusable FDA UDI
Device Name
Regular FDA UDI
Model / Reference
Reusable Regular FDA UDI
Description
Regular FDA UDI

Identifiers

Primary DI / UDI-DI
00860010693100 FDA UDI
FDA Product Code
FRZ FDA UDI
GMDN Term
Inflatable patient transfer sliding mattress, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6775 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Inflatable patient transfer sliding mattress, reusable

PPS Glide by Patient Positioning Systems, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Inflatable patient transfer sliding mattress, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 68956890-2d6d-4a31-8ff7-a87970f9d852 33 fields · synced May 30, 2026