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Procure

FDA UDI

Class II (US FDA UDI)

by Proactive Medical Products

Identity

Trade Name
Procure FDA UDI
Generic Name
Basic electric home bed FDA UDI
Device Name
Procure Full Electric Bed,spring deck with full rails FDA UDI
Model / Reference
PMFEBFRTM FDA UDI
Description
Procure Full Electric Bed,spring deck with full rails FDA UDI

Identifiers

Catalog Number
PMFEBFRTM FDA UDI
Primary DI / UDI-DI
05060488571541 FDA UDI
FDA Product Code
FNL FDA UDI
GMDN Term
Basic electric home bed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5100 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 80 Inch FDA UDI
Width — 36 Inch FDA UDI
Height — 24 Inch FDA UDI

Category: Basic electric home bed

Procure by Proactive Medical Products — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic electric home bed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 484e4e13-467f-456c-9354-dd170b96418e 36 fields · synced Jun 8, 2026