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Hoggi®

FDA UDI

Class I (US FDA UDI)

by Hoggi GmbH

Identity

Trade Name
HOGGI® FDA UDI
Generic Name
Assistive pushchair FDA UDI
Device Name
BINGO Evolution seat unit size 2XL, black dull matt FDA UDI
Model / Reference
3235-2000-032 FDA UDI
Description
BINGO Evolution seat unit size 2XL, black dull matt FDA UDI

Identifiers

Primary DI / UDI-DI
04047349075906 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

Yes

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

Yes

FDA UDI

Category: Assistive pushchair

Hoggi® by Hoggi GmbH — 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
Hoggi GmbH

Sources (1)

  • FDA UDI 23382543-6cb4-4f2a-bfd1-142d0b44958f 34 fields · synced Jun 8, 2026