Identity
- Trade Name
- DOUBLEFLO FDA UDI
- Generic Name
- Electrical mains power cable FDA UDI
- Device Name
- POWER CORD FOR EU FDA UDI
- Model / Reference
- A FDA UDI
- Description
- POWER CORD FOR EU FDA UDI
Identifiers
- Catalog Number
- 72205368 FDA UDI
- Primary DI / UDI-DI
- 03661379196083 FDA UDI
- 510(k) Number
- K221919 FDA UDI
- FDA Product Code
- HRX FDA UDI
- GMDN Term
- Electrical mains power cable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.1100 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
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Electrical mains power cable
Doubleflo by Hemodia — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Hemodia
Sources (1)
- FDA UDI 3963b4ad-1072-46ac-afa2-6c64614ae314 35 fields · synced Jun 8, 2026