Identity
- Trade Name
- Deymed Li-ion Battery FDA UDI
- Generic Name
- Secondary battery FDA UDI
- Device Name
- Neurofeedback device accessories FDA UDI
- Model / Reference
- 3.7V 2500mAh 16650 FDA UDI
- Description
- Neurofeedback device accessories FDA UDI
Identifiers
- Catalog Number
- 45-361 FDA UDI
- Primary DI / UDI-DI
- 08592566453618 FDA UDI
- FDA Product Code
- HCC FDA UDI
- GMDN Term
- Secondary battery FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5050 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
No
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
No
FDA UDI
Category: Secondary battery
Deymed Li-ion Battery by DEYMED Diagnostic s.r.o. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- M Battery — Advanced Bionics · Class III
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
- DEYMED Diagnostic s.r.o.
Sources (1)
- FDA UDI 2b7b8532-43c3-41ba-9549-14166e95a5a2 35 fields · synced May 31, 2026