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Probe Hooked Triple 37x0.75mm 1pc
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 73605-190/1
Identity
- Trade Name
- Probe Hooked Triple 37x0.75mm 1pc EUDAMEDAmbu FDA UDI
- Generic Name
- Nerve-locating system probe, single-use FDA UDI
- Device Name
- Ambu ® Triple Hooked Probe EUDAMEDAmbu ® Triple Hooked Probe 37x0.75mm 1pc FDA UDI
- Model / Reference
- 73605-190/1 EUDAMEDFDA UDI
- Description
- Ambu ® Triple Hooked Probe 37x0.75mm 1pc FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08718375869338 EUDAMEDFDA UDI
- Basic UDI-DI
- B-08718375869338 EUDAMED
- FDA Product Code
- GXZ FDA UDI
- EMDN Code
- Z12101185 PERIPHERAL OR CENTRAL NEURO STIMULATION AND ASSESSMENT INSTRUMENTS - CONSUMABLES EUDAMED
- GMDN Term
- Nerve-locating system probe, single-use FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 882.1350 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
Yes
FDA UDI
Probe Hooked Triple 37x0.75mm 1pc 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-08718375869338 | 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 637b7482-dfe9-47a5-b307-dab88475071f 61 fields · synced Jun 19, 2026
- FDA UDI 970e6d9a-a726-49f1-88e5-f98fdabc3f50 34 fields · synced May 30, 2026