Identity
- Trade Name
- Neo/Inf Intub CO2 Line LTerm EUDAMEDMicrostream Advance Neonatal-Infant Intubated CO2 Filter Line FDA UDI
- Generic Name
- Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI
- Device Name
- Microstream Advanced EUDAMEDMicrostream Advance Neonatal-Infant Intubated CO2 Filter Line, Extended Duration FDA UDI
- Model / Reference
- 989803204531 EUDAMEDNeo/Inf Intub CO2 Line LTerm FDA UDI
- Description
- Microstream Advance Neonatal-Infant Intubated CO2 Filter Line, Extended Duration FDA UDI
Identifiers
- Catalog Number
- 989803204531 FDA UDI
- Primary DI / UDI-DI
- 20884838093137 EUDAMEDFDA UDI
- Basic UDI-DI
- 0884838BM547TD EUDAMED
- Unit of Use DI
- 00884838093133 EUDAMED
- FDA Product Code
- CCK FDA UDI
- EMDN Code
- Z1203020202 TRANSPORTABLE/PORTABLE MULTI–PARAMETER PATIENT MONITORS EUDAMED
- GMDN Term
- Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI
Classification
- Device Class
- Class I 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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Neo/Inf Intub CO2 Line LTerm by Philips Medical Systems — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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 | 0884838BM547TD | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Philips Medical Systems
- EUDAMED SRN
- US-MF-000002321
- Authorised Representative
- Philips Medical Systems Nederland B.V. NL-AR-000001422
Sources (2)
- EUDAMED ff4a6ca7-6b5f-4c79-829b-7af9ff370f5b 61 fields · synced Jul 27, 2026
- FDA UDI 1bc83882-3803-4843-9aca-1a7a765bbd7b 36 fields · synced May 30, 2026