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Zephyr Patient Positioning and Transfer System
FDA UDIClass II (US FDA UDI)
by Diacor Inc.
Identity
- Trade Name
- Zephyr Patient Positioning and Transfer System FDA UDI
- Generic Name
- Patient transfer system, powered FDA UDI
- Device Name
- Zephyr Blower Kit for 110-120v, UL Listed FDA UDI
- Model / Reference
- ZBL-3 FDA UDI
- Description
- Zephyr Blower Kit for 110-120v, UL Listed FDA UDI
Identifiers
- Primary DI / UDI-DI
- B237ZBL30 FDA UDI
- 510(k) Number
- K121929 FDA UDI
- FDA Product Code
- FRZ FDA UDI
- GMDN Term
- Patient transfer system, powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6775 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
Yes
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Zephyr Patient Positioning and Transfer System by Diacor Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
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
- Diacor Inc.
Sources (1)
- FDA UDI 581295ae-9251-4460-bf9b-84683e30a50d 35 fields · synced May 31, 2026