Identity
- Trade Name
- COSMED FDA UDI
- Generic Name
- Indirect calorimeter FDA UDI
- Device Name
- This device is intended for use in clinical and research application to measure oxygen uptake. FDA UDI
- Model / Reference
- Fitmate GS FDA UDI
- Description
- This device is intended for use in clinical and research application to measure oxygen uptake. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 18052400180362 FDA UDI
- 510(k) Number
- K071533 FDA UDI
- FDA Product Code
- BZL FDA UDI
- GMDN Term
- Indirect calorimeter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.1730 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: Indirect calorimeter
Cosmed by C O S M E D Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Indirect calorimeter.
- ReeVue — KORR MEDICAL TECHNOLOGIES, INC. · Class II
- Microlife — MICROLIFE USA, INC. · Class II
- COSMED — C O S M E D SRL · Class II
Cleared under the same submission
K071533 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 |
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Manufacturer
- Manufacturer
- C O S M E D Srl
Sources (1)
- FDA UDI 34605285-37a4-4888-a184-8ce36c78ade7 35 fields · synced Jun 8, 2026