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Inductive Belt Kit - St3
EUDAMEDFDA UDIClass I (EU MDR)
Ref 9002GModel 9XXX, 9XXX-LXX, 501-0261-X series
by S.L.P. Ltd.
Identity
- Trade Name
- INDUCTIVE BELT KIT - ST3 EUDAMEDGrass FDA UDI
- Generic Name
- Electrode/transducer strap, reusable FDA UDI
- Device Name
- Inductive Sensors EUDAMED
- Model / Reference
- 9XXX, 9XXX-LXX, 501-0261-X series EUDAMED9002G EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 07290012186349 EUDAMEDFDA UDI
- Basic UDI-DI
- 7290001671EF001L7 EUDAMED
- EMDN Code
- Z1399 NON-SPECIFIC CONSUMABLES FOR DIAGNOSTIC INSTRUMENTS - OTHER EUDAMED
- GMDN Term
- Electrode/transducer strap, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
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
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Inductive Belt Kit - St3 by S.L.P. Ltd. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 7290001671EF001L7 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- S.L.P. Ltd.
- EUDAMED SRN
- IL-MF-000016600
- Authorised Representative
- Arazy Group GmbH DE-AR-000007685
Sources (2)
- EUDAMED 51cb6be4-c78b-4fe9-a805-a2e49d9eff99 61 fields · synced Jun 19, 2026
- FDA UDI 422e8d72-0145-4017-8910-9a55ee0eb08d 32 fields · synced May 30, 2026