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Ambu® Subdermal Twisted Pair Corkscrew
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 74820-60/12
Identity
- Trade Name
- Ambu® Subdermal Twisted Pair Corkscrew EUDAMEDAmbu FDA UDI
- Generic Name
- Electromyographic needle electrode, single-use FDA UDI
- Device Name
- Ambu® Subdermal Twisted Pair Corkscrew EUDAMEDAmbu® Subdermal Twisted Pair Corkscrew 2.0m twisted wire 12pairs & PC FDA UDI
- Model / Reference
- 74820-60/12 EUDAMEDFDA UDI
- Description
- Ambu® Subdermal Twisted Pair Corkscrew 2.0m twisted wire 12pairs & PC FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08718375869246 EUDAMEDFDA UDI
- Basic UDI-DI
- B-08718375869246 EUDAMED
- FDA Product Code
- GXZ FDA UDIIKT FDA UDI
- EMDN Code
- N01010202 EEG EXTRACRANIC 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 UDI890.1385 FDA UDI
- Market of Registration
- Netherlands 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
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
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
No
FDA UDI
MR Unsafe FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 0.60 Millimeter FDA UDILength — 2 Meter FDA UDINeedle Gauge — 23 Gauge FDA UDI
Ambu® Subdermal Twisted Pair Corkscrew by Technomed Europe — 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-08718375869246 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Technomed Europe
- EUDAMED SRN
- NL-MF-000000064
Sources (2)
- EUDAMED 546b8c7f-4544-4c84-8879-d1fa0ba03bce 61 fields · synced Jul 19, 2026
- FDA UDI dedd56b5-d76f-4a00-acec-7700ccab7a52 35 fields · synced May 30, 2026