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Asp Global Primo

FDA UDI

Class I (US FDA UDI)

by Asp Global, LLC

Identity

Trade Name
ASP GLOBAL PRIMO FDA UDI
Generic Name
Inflatable patient transfer sliding mattress, single-use FDA UDI
Device Name
AIRFLOAT AIR TRANSFER MATTRESS SET W/UPD FDA UDI
Model / Reference
AFTS01 FDA UDI
Description
AIRFLOAT AIR TRANSFER MATTRESS SET W/UPD FDA UDI

Identifiers

Primary DI / UDI-DI
00840216128804 FDA UDI
FDA Product Code
FMR FDA UDI
FMP FDA UDI
KME FDA UDI
GMDN Term
Inflatable patient transfer sliding mattress, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6785 FDA UDI
880.6450 FDA UDI
880.6060 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

Yes

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: Inflatable patient transfer sliding mattress, single-use

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

Similar devices

Also classified as Inflatable patient transfer sliding mattress, 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 305509e7-b5f3-442f-b8d6-d8da5e874cdb 33 fields · synced Jun 6, 2026