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Piezo Crystal Effort Sensor - Double Buckle / PL connector
EUDAMEDFDA UDIClass I (EU MDR)
Ref 1374Model 13XX, 612XX seriesRef 601011
by S.L.P. Ltd.
Identity
- Trade Name
- Piezo Crystal Effort Sensor - Double Buckle / PL connector EUDAMEDPiezo Crystal Effort EUDAMEDSleepsense FDA UDI
- Generic Name
- Polysomnography analyser FDA UDI
- Device Name
- Effort Sensors EUDAMED
- Model / Reference
- 13XX, 612XX series EUDAMED1374 EUDAMEDFDA UDI601011 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07290012186691 EUDAMEDFDA UDI07290016716078 EUDAMED
- Basic UDI-DI
- 7290008986EF001VK EUDAMED
- 510(k) Number
- K042253 FDA UDI
- FDA Product Code
- MNR FDA UDI
- EMDN Code
- Z1399 NON-SPECIFIC CONSUMABLES FOR DIAGNOSTIC INSTRUMENTS - OTHER EUDAMED
- GMDN Term
- Polysomnography analyser FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 868.2375 FDA UDI
- 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
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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Piezo Crystal Effort Sensor - Double Buckle / PL connector 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 | 7290008986EF001VK | 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 (3)
- EUDAMED 90eb3e0c-3ba4-4cb2-a600-8117fba87f06 61 fields · synced Sep 18, 2026
- EUDAMED 89099149-4587-4df1-adbf-bce86038752d 61 fields · synced May 17, 2026
- FDA UDI 8d79d5fc-a083-4d8b-89f4-8e8f39437b8f 33 fields · synced May 30, 2026