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Stay Safe

FDA UDI

Class I (US FDA UDI)

by Pedicraft, Inc.

Identity

Trade Name
Stay Safe FDA UDI
Generic Name
Manual hospital bed FDA UDI
Device Name
Stay Safe Bed HE HA FDA UDI
Model / Reference
34812 FDA UDI
Description
Stay Safe Bed HE HA FDA UDI

Identifiers

Primary DI / UDI-DI
00766923348123 FDA UDI
FDA Product Code
FNJ FDA UDI
GMDN Term
Manual hospital bed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5120 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

Yes

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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Manual hospital bed

Stay Safe by Pedicraft, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual hospital bed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pedicraft, Inc.

Sources (1)

  • FDA UDI 5883b0be-48e8-42d2-981b-16b58a1bfeb7 34 fields · synced May 30, 2026