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LoFlo CO2 Sampling O2 Delivery Cannula w/Dehumidification Tubing ADULT ORAL/NAS…
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 3471ADH-00
Identity
- Trade Name
- LoFlo CO2 Sampling O2 Delivery Cannula w/Dehumidification Tubing ADULT ORAL/NASAL EUDAMEDLoFlo Accessories FDA UDI
- Generic Name
- Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI
- Device Name
- Sidestream Accessories EUDAMEDLoFlo CO2 Sampling O2 Delivery Cannula with Dehumidification Tubing ADULT ORAL/NASAL FDA UDI
- Model / Reference
- 3471ADH-00 EUDAMEDFDA UDI
- Description
- LoFlo CO2 Sampling O2 Delivery Cannula with Dehumidification Tubing ADULT ORAL/NASAL FDA UDI
Identifiers
- Catalog Number
- 3471ADH-00 FDA UDI
- Primary DI / UDI-DI
- 00884838014015 EUDAMEDFDA UDI
- Basic UDI-DI
- 0884838BM630SZ EUDAMED
- FDA Product Code
- CCK FDA UDI
- EMDN Code
- Z1203020485 GASEOUS EXCHANGE MONITORING INSTRUMENTS - CONSUMABLES EUDAMED
- GMDN Term
- Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 868.1400 FDA UDI
- Market of Registration
- Austria EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
LoFlo CO2 Sampling O2 Delivery Cannula w/Dehumidification Tubing ADULT ORAL/NAS… by Respironics Novametrix, LLC — Class IIa — MDR, FDA UDI — listed in…
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0884838BM630SZ | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Respironics Novametrix, LLC
- EUDAMED SRN
- US-MF-000007951
- Authorised Representative
- Philips Medical Systems Nederland B.V. NL-AR-000001422
Sources (2)
- EUDAMED 9e251fb4-67b0-4956-9d50-2b374f14beef 61 fields · synced Jul 25, 2026
- FDA UDI a25bb212-8d06-4a9c-bd7b-857f7ced732e 35 fields · synced May 30, 2026