Identity
- Trade Name
- PROEMG FDA UDI
- Generic Name
- Electromyographic needle electrode, single-use FDA UDI
- Device Name
- EMG Needle Electrode EUDAMEDConcentric Needle, Non-Wired, 25mm(L)x0.30mm(D), White Hub FDA UDI
- Model / Reference
- BC2530 EUDAMEDFDA UDI
- Description
- Concentric Needle, Non-Wired, 25mm(L)x0.30mm(D), White Hub FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08809083944520 EUDAMEDFDA UDI
- Basic UDI-DI
- B-08809083944520 EUDAMED
- 510(k) Number
- K152984 FDA UDI
- FDA Product Code
- GXZ FDA UDI
- EMDN Code
- N010101 ELECTROMYOGRAPHIC ELECTRODES EUDAMED
- GMDN Term
- Electromyographic needle electrode, single-use FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 882.1350 FDA UDI
- Market of Registration
- Spain EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Yes
FDA UDI
EMG Needle Electrode by Bio Protech Inc. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-08809083944520 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Bio Protech Inc.
- EUDAMED SRN
- KR-MF-000012687
- Authorised Representative
- Meridius Medical Europe Limited IE-AR-000004258
Sources (2)
- EUDAMED f82a80e4-50be-49a3-85fb-c71167a55513 61 fields · synced Jul 9, 2026
- FDA UDI 62d0014a-70e2-465f-9588-12388da784d2 35 fields · synced May 27, 2026