Identity
- Trade Name
- RPSII FDA UDI
- Generic Name
- Portable/mobile rechargeable battery pack FDA UDI
- Device Name
- RPSII - DC CABLE VPAP IV FDA UDI
- Model / Reference
- 24960 FDA UDI
- Description
- RPSII - DC CABLE VPAP IV FDA UDI
Identifiers
- Catalog Number
- 24960 FDA UDI
- Primary DI / UDI-DI
- 00619498249602 FDA UDI
- 510(k) Number
- K071171 FDA UDI
- FDA Product Code
- BZD FDA UDI
- GMDN Term
- Portable/mobile rechargeable battery pack FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5905 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Rpsii by Resmed Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K071171 also covers:
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 II | Pending data |
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Manufacturer
- Manufacturer
- Resmed Pty Ltd
Sources (1)
- FDA UDI 3a1bfb1c-380a-4c51-bced-9c72098b696f 37 fields · synced Jun 1, 2026