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Obi

FDA UDI

Class I (US FDA UDI)

by Ormesa Srl

Identity

Trade Name
OBI FDA UDI
Generic Name
Assistive pushchair FDA UDI
Device Name
Obi is a pushchair suitable for users with important functional impairments, with little or no control of the head and trunk, with little or no functional capacity, who need a particularly robust structure to be used mainly outdoors. FDA UDI
Model / Reference
OBI-4 RUOTE NON ESTRAIBILI FDA UDI
Description
Obi is a pushchair suitable for users with important functional impairments, with little or no control of the head and trunk, with little or no functional capacity, who need a particularly robust structure to be used mainly outdoors. FDA UDI

Identifiers

Primary DI / UDI-DI
08055715704561 FDA UDI
FDA Product Code
INM FDA UDI
GMDN Term
Assistive pushchair FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3100 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Assistive pushchair

Obi by Ormesa Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assistive pushchair.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ormesa Srl

Sources (1)

  • FDA UDI bde0a5c9-c48f-4d30-a85a-319d0829d041 33 fields · synced May 30, 2026