Identity
- Trade Name
- Grass FDA UDI
- Generic Name
- Polysomnography analyser FDA UDI
- Model / Reference
- 1330A-Kit FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07290013819789 FDA UDI
- GMDN Term
- Polysomnography analyser FDA UDI
Classification
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Category: Polysomnography analyser
Grass by S.l.p. Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Polysomnography analyser.
- Sleepware — Respironics, Inc. · Class II
- Sleepsense — S. L. P. SCIENTIFIC LABORATORY PRODUCTS LTD · Class II
- Onera STS — Onera B.V. · Class II
- Nox T3® System with WristOx2 — Nox Medical ehf. · Class II
- Onera STS — Onera B.V. · Class II
- Sleepware — Respironics, Inc. · Class II
- Embla — S. L. P. SCIENTIFIC LABORATORY PRODUCTS LTD · Class II
- Embla — S. L. P. SCIENTIFIC LABORATORY PRODUCTS LTD · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | N/A | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- S.l.p. Inc.
Sources (1)
- FDA UDI b67e585b-2a12-4dea-9fc3-1b6d0beeb8c3 32 fields · synced May 30, 2026