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REMstar Pro C-Flex+, w/HT Humid System One 60 Series INT
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref IN461TSModel REMstar Pro C-Flex+
Identity
- Trade Name
- REMstar Pro C-Flex+, w/HT Humid System One 60 Series INT EUDAMEDREMstar System One 60 Series FDA UDI
- Generic Name
- Home CPAP unit FDA UDI
- Device Name
- REMstar Pro C-Flex+, with Heated Tube Humidifier, System One 60 Series, International FDA UDI
- Model / Reference
- REMstar Pro C-Flex+ EUDAMEDIN461TS EUDAMEDREMstar Pro C-Flex+, w/H Tube Humid, 60 Series, INTL FDA UDI
- Description
- REMstar Pro C-Flex+, with Heated Tube Humidifier, System One 60 Series, International FDA UDI
Identifiers
- Catalog Number
- IN461TS FDA UDI
- Primary DI / UDI-DI
- 00606959030275 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00606959030275 EUDAMED
- FDA Product Code
- BZD FDA UDI
- EMDN Code
- Z12030102 CONTINUOUS POSITIVE PRESSURE EQUIPMENT EUDAMED
- GMDN Term
- Home CPAP unit FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 868.5905 FDA UDI
- Market of Registration
- Austria EUDAMED
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
REMstar Pro C-Flex+, w/HT Humid System One 60 Series INT by Respironics, Inc. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-00606959030275 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Respironics Inc.
- EUDAMED SRN
- US-MF-000002301
- Authorised Representative
- Respironics Deutschland GmbH & Co.KG DE-AR-000006164
Sources (3)
- EUDAMED c00a48c3-168d-4bc6-9bb9-cae75e419988 61 fields · synced Jul 10, 2026
- FDA UDI ee4e2c35-b7dd-4f95-8be4-7575f037e02b 37 fields · synced May 30, 2026
- EUDAMED 5766a428-71c8-412a-b835-b95978870ef9 61 fields · synced Jul 10, 2026