Identity
- Trade Name
- Fisher & Paykel Healthcare FDA UDI
- Generic Name
- Digital storage media FDA UDI
- Device Name
- F&P InfoUSB FDA UDI
- Model / Reference
- 900ICON203 FDA UDI
- Description
- F&P InfoUSB FDA UDI
Identifiers
- Catalog Number
- 900ICON203 FDA UDI
- Primary DI / UDI-DI
- 09420012424266 FDA UDI
- FDA Product Code
- OUG FDA UDI
- GMDN Term
- Digital storage media FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6310 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Digital storage media
Fisher & Paykel Healthcare by Fisher & Paykel Healthcare, Inc. — 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
- Fisher & Paykel Healthcare, Inc.
Sources (1)
- FDA UDI ee17602d-22cf-4669-9dda-72040c839b04 36 fields · synced Jun 6, 2026