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Primo/Asp Medical

FDA UDI

Class I (US FDA UDI)

by Asp Global, LLC

Identity

Trade Name
PRIMO/ASP MEDICAL FDA UDI
Generic Name
Patient transfer/turning sheet, single-use FDA UDI
Device Name
GUIDE & GLIDE TURN SHEET PLUS, 36"X60", W/TOP & SIDE HANDLES, PURPLE/GRAY, 1EA/BG, 24BG/CS FDA UDI
Model / Reference
GGS3660TSH FDA UDI
Description
GUIDE & GLIDE TURN SHEET PLUS, 36"X60", W/TOP & SIDE HANDLES, PURPLE/GRAY, 1EA/BG, 24BG/CS FDA UDI

Identifiers

Primary DI / UDI-DI
00840216122680 FDA UDI
FDA Product Code
FMR FDA UDI
GMDN Term
Patient transfer/turning sheet, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6785 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Patient transfer/turning sheet, single-use

Primo/Asp Medical by Asp Global, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient transfer/turning sheet, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Asp Global, LLC

Sources (1)

  • FDA UDI 86147608-a413-44b1-96f6-3cde95cc96ff 33 fields · synced May 30, 2026