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Selectis

FDA UDI

Class II (US FDA UDI)

by Emerald Supplies Inc

Identity

Trade Name
Selectis FDA UDI
Generic Name
Low-air-loss bed FDA UDI
Model / Reference
61062 FDA UDI

Identifiers

Primary DI / UDI-DI
B572610620 FDA UDI
FDA Product Code
FNM FDA UDI
GMDN Term
Low-air-loss bed 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

Yes

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: Low-air-loss bed

Selectis by Emerald Supplies Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Low-air-loss bed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c0a0e103-7968-4e07-b753-df4b21e0d690 32 fields · synced May 30, 2026