Identity
- Trade Name
- HOGGI® FDA UDI
- Generic Name
- Assistive pushchair FDA UDI
- Device Name
- BINGO Evo OT-PLUS seat size 2, black dull matt FDA UDI
- Model / Reference
- 3233-3003-032 FDA UDI
- Description
- BINGO Evo OT-PLUS seat size 2, black dull matt FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04047349099070 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
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Hoggi GmbH
Sources (1)
- FDA UDI db76a7a2-b038-4fdc-8098-8dea15e76328 34 fields · synced Jun 8, 2026