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Sizewise

FDA UDI

Class II (US FDA UDI)

by Sizewise Rentals, L.l.c.

Identity

Trade Name
Sizewise FDA UDI
Generic Name
Flotation therapy bed, adult FDA UDI
Device Name
Pediatric Gel Bassinet 18" x 22" x 1" FDA UDI
Model / Reference
7770-PGI11822 FDA UDI
Description
Pediatric Gel Bassinet 18" x 22" x 1" FDA UDI

Identifiers

Primary DI / UDI-DI
00845699003235 FDA UDI
FDA Product Code
FNM FDA UDI
GMDN Term
Flotation therapy bed, adult 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Flotation therapy bed, adult

Sizewise by Sizewise Rentals, L.l.c. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flotation therapy bed, adult.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 26364b01-1e69-4d0f-8b28-597b9eb59ebe 33 fields · synced Jun 6, 2026