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Microstream Advance

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Microstream Advance FDA UDI
Generic Name
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI
Device Name
Adult-Pediatric Intubated CO2 Filter Line;High Humidity FDA UDI
Model / Reference
ZMVAIHH FDA UDI
Description
Adult-Pediatric Intubated CO2 Filter Line;High Humidity FDA UDI

Identifiers

Primary DI / UDI-DI
20884521762265 FDA UDI
510(k) Number
K181467 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
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 Unsafe FDA UDI

Dimensions & Sizes

Size
Length — 2 Meter FDA UDI

Category: Nasal oxygen cannula, carbon-dioxide-sampling

Microstream Advance by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal oxygen cannula, carbon-dioxide-sampling.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI bb06ca9b-3dc3-4201-af99-f5a5a109efba 37 fields · synced Jun 7, 2026