Identity
- Trade Name
- NatureSpirit FDA UDI
- Generic Name
- Pulse oximeter, line-powered FDA UDI
- Device Name
- Fingertip Oximeter, rechargeable battery FDA UDI
- Model / Reference
- CMS-50dl FDA UDI
- Description
- Fingertip Oximeter, rechargeable battery FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00897037001083 FDA UDI
- FDA Product Code
- DQA FDA UDI
- GMDN Term
- Pulse oximeter, line-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2700 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
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Pulse oximeter, line-powered
NatureSpirit by Simpro — 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
- Simpro
Sources (1)
- FDA UDI d7daaea2-a8e0-4253-8c27-26a65da5dc40 34 fields · synced Jun 6, 2026