Nihon Kohden Life Scope G7 Bedside Monitoring System
FDA UDIEUDAMEDClass II (US FDA UDI)
Identity
- Trade Name
- Battery Pack SB-970P EUDAMEDNihon Kohden Life Scope G7 Bedside Monitoring System FDA UDI
- Generic Name
- Portable/mobile rechargeable battery pack FDA UDI
- Device Name
- General-purpose multi-parameter bedside monitor EUDAMEDBattery pack (for CU-171R, CU-172R) FDA UDI
- Model / Reference
- SB-970P SB-970P-CL SB-970P-CL-30 EUDAMEDSB-970P FDA UDI
- Description
- Battery pack (for CU-171R, CU-172R) FDA UDI
Identifiers
- Catalog Number
- SB-970P FDA UDI
- Primary DI / UDI-DI
- 04931921023631 EUDAMEDFDA UDI
- Basic UDI-DI
- 4931921MD10004BD EUDAMED
- FDA Product Code
- MHX FDA UDI
- EMDN Code
- Z1203020285 MULTI-PARAMETER MONITORS - CONSUMABLES EUDAMED
- GMDN Term
- Portable/mobile rechargeable battery pack FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 870.1025 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
Implantable
No
Reusable
No
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
No
Serial Number
Yes
Expiration Date
No
Manufacturing Date
No
Category: Portable/mobile rechargeable battery pack
Nihon Kohden Life Scope G7 Bedside Monitoring System by Nihon Kohden Corp. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED
Similar devices
Also classified as Portable/mobile rechargeable battery pack.
- R&D Batteries, Inc. — R & D BATTERIES, INC. · Class I
- Unipower — Unipower Corp. · Class II
- ALPHA SOURCE BATTERY — ALPHA SOURCE INC. · Class II
- ALPHA SOURCE BATTERY — ALPHA SOURCE INC. · Class III
- R&D Batteries, Inc. — R & D BATTERIES, INC. · Class I
- R&D Batteries, Inc. — R & D BATTERIES, INC. · Class II
- R&D Batteries, Inc. — R & D BATTERIES, INC. · Class I
- R&D Batteries, Inc. — R & D BATTERIES, INC. · Class II
Authorization Coverage (2 countries)
Regulatory Authorizations
MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| 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 (2)
- FDA UDI f7bfd0bb-1e28-48f2-9e00-035639f01373 35 fields · synced Jun 19, 2026
- EUDAMED 83aa8a19-ff3b-4b01-96e6-5b10a7b9d346 61 fields · synced Jun 19, 2026