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Microstream Advance

FDA UDI

Class II (US FDA UDI)

by Oridion Medical 1987 Ltd.

Identity

Trade Name
Microstream Advance FDA UDI
Generic Name
Gas-sampling/monitoring respiratory tubing, single-use FDA UDI
Device Name
Pediatric Nasal CO2 Filter Line; Short-term use: Procedural/Emergency FDA UDI
Model / Reference
MVPN FDA UDI
Description
Pediatric Nasal CO2 Filter Line; Short-term use: Procedural/Emergency FDA UDI

Identifiers

Primary DI / UDI-DI
20884521771755 FDA UDI
FDA Product Code
CCK FDA UDI
GMDN Term
Gas-sampling/monitoring respiratory tubing, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1400 FDA UDI
Commercial Distribution
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

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Length — 2 Meter FDA UDI

Category: Gas-sampling/monitoring respiratory tubing, single-use

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

Similar devices

Also classified as Gas-sampling/monitoring respiratory tubing, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5b9123cf-2469-4340-9e0a-3494fed7c3bf 36 fields · synced Jun 1, 2026