Identity
- Trade Name
- Greentek FDA UDI
- Generic Name
- Electroencephalographic electrode cap, single-use FDA UDI
- Model / Reference
- Flex-cap BM-FC03-23C1 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06970295340669 FDA UDI
- FDA Product Code
- GXY FDA UDI
- GMDN Term
- Electroencephalographic electrode cap, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1320 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Safe FDA UDI
Category: Electroencephalographic electrode cap, single-use
Greentek by Wuhan Greentek Pty Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Greentek — Wuhan Greentek Pty Ltd. · Class II
- Greentek — Wuhan Greentek Pty Ltd. · Class II
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
- Wuhan Greentek Pty Ltd.
Sources (1)
- FDA UDI 40c33a86-f739-49e7-87b4-a442c82047d2 32 fields · synced May 30, 2026