Identity
- Trade Name
- Spacelabs FDA UDI
- Generic Name
- Patient monitoring system module rack FDA UDI
- Device Name
- INTEGRATED MODULE HOUSING FDA UDI
- Model / Reference
- UltraviewSL FDA UDI
- Description
- INTEGRATED MODULE HOUSING FDA UDI
Identifiers
- Catalog Number
- 91493 FDA UDI
- Primary DI / UDI-DI
- 10841522100260 FDA UDI
- 510(k) Number
- K842616 FDA UDI
- FDA Product Code
- DSI FDA UDI
- GMDN Term
- Patient monitoring system module rack FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1025 FDA UDI
- 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
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Patient monitoring system module rack
Spacelabs by Spacelabs Healthcare (washington), Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K842616 also covers:
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 | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Spacelabs Healthcare (washington), Inc
Sources (1)
- FDA UDI ace61001-eb7b-4332-875d-a91c5d140628 36 fields · synced May 30, 2026