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Air Mattress, Compact Dial Operated Pump, Single Cell

FDA UDI

Class II (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Air Mattress, Compact Dial Operated Pump, Single Cell FDA UDI
Generic Name
Basic bed mattress FDA UDI
Model / Reference
10441 FDA UDI

Identifiers

Primary DI / UDI-DI
00616784044118 FDA UDI
FDA Product Code
FNM FDA UDI
GMDN Term
Basic bed mattress FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5550 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Basic bed mattress

Air Mattress, Compact Dial Operated Pump, Single Cell by Dynarex Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic bed mattress.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI e0b6afbb-a31a-4234-acd1-059a7d9e919d 32 fields · synced May 29, 2026