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Microstream

FDA UDI

Class II (US FDA UDI)

by Oridion Medical 1987 Ltd.

Identity

Trade Name
Microstream FDA UDI
Generic Name
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI
Device Name
Smart CapnoLine Plus O2 Adult/Intermediate CO2 Oral/Nasal Sampling Set with O2 Tubing FDA UDI
Model / Reference
015283 FDA UDI
Description
Smart CapnoLine Plus O2 Adult/Intermediate CO2 Oral/Nasal Sampling Set with O2 Tubing FDA UDI

Identifiers

Primary DI / UDI-DI
20884521552316 FDA UDI
FDA Product Code
CCK FDA UDI
GMDN Term
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1400 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Microstream by Oridion Medical 1987 Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8975fd53-2a52-4309-9bae-e1053bf235ef 35 fields · synced Jun 6, 2026