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Mobile Patient Bed

FDA UDI

Class I (US FDA UDI)

by Johnson & Johnson Surgical Vision, Inc.

Identity

Trade Name
MOBILE PATIENT BED FDA UDI
Generic Name
Ophthalmic operating table, electromechanical FDA UDI
Device Name
RISER ADAPTER, HEADREST, MPB, US FDA UDI
Model / Reference
0160-5432 FDA UDI
Description
RISER ADAPTER, HEADREST, MPB, US FDA UDI

Identifiers

Catalog Number
0160-5432 FDA UDI
Primary DI / UDI-DI
05050474824935 FDA UDI
FDA Product Code
FQO FDA UDI
GMDN Term
Ophthalmic operating table, electromechanical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 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

Category: Ophthalmic operating table, electromechanical

Mobile Patient Bed by Johnson & Johnson Surgical Vision, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic operating table, electromechanical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c93b3129-11c7-4062-b2b4-a94c01833107 35 fields · synced Jun 9, 2026