← Back to catalogue
Nihon Kohden Life Scope G5 Bedside Monitoring System, Nihon Kohden Life Scope G7
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Nihon Kohden Life Scope G5 Bedside Monitoring System, Nihon Kohden Life Scope G7 FDA UDI
- Generic Name
- General-purpose multi-parameter bedside monitor FDA UDI
- Device Name
- Side option board (for CU-152R, CU-171R, CU-172R) FDA UDI
- Model / Reference
- QI-152P FDA UDI
- Description
- Side option board (for CU-152R, CU-171R, CU-172R) FDA UDI
Identifiers
- Catalog Number
- QI-152P FDA UDI
- Primary DI / UDI-DI
- 04931921002117 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: General-purpose multi-parameter bedside monitor
Nihon Kohden Life Scope G5 Bedside Monitoring System, Nihon Kohden Life Scope G7 by Nihon Kohden Corp. — Class II — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as General-purpose multi-parameter bedside monitor.
- SpO2 Adapter cable — Orantech Inc. · Class I
- Welch Allyn, Inc. — Welch Allyn, Inc. · Class II
- Welch Allyn, Inc. — Welch Allyn, Inc. · Class II
- Flying-V cuff LARGE — CNSystems Medizintechnik GmbH · Class II
- Expression MR200 Accessories — Philips DS North America LLC · Class II
- IBP Adapter Cable — Orantech Inc. · Class I
- LiDCO — LIDCO LIMITED · Class II
- LiDCO — LIDCO LIMITED · 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 | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Nihon Kohden Corp.
Sources (1)
- FDA UDI ca71edf0-7ed7-409d-a807-dabb3e781d3a 34 fields · synced May 31, 2026