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Nihon Kohden Life Scope G7 Bedside Monitoring System
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Nihon Kohden Life Scope G7 Bedside Monitoring System FDA UDI
- Generic Name
- General-purpose multi-parameter bedside monitor FDA UDI
- Device Name
- Stand (for CU-171R, CU-172R) FDA UDI
- Model / Reference
- DM-150P FDA UDI
- Description
- Stand (for CU-171R, CU-172R) FDA UDI
Identifiers
- Catalog Number
- DM-150P FDA UDI
- Primary DI / UDI-DI
- 04931921004784 FDA UDI
- FDA Product Code
- MHX FDA UDI
- GMDN Term
- General-purpose multi-parameter bedside monitor 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: General-purpose multi-parameter bedside monitor
Nihon Kohden Life Scope G7 Bedside Monitoring System by Nihon Kohden Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- Nihon Kohden Corp.
Sources (1)
- FDA UDI 25c8eda7-161e-4a37-86de-7253e56fa633 34 fields · synced May 30, 2026