← Back to catalogue

Microstream

FDA UDI

Class II (US FDA UDI)

by Oridion Medical 1987 Ltd.

Identity

Trade Name
Microstream FDA UDI
Generic Name
Gas-sampling/monitoring respiratory tubing, single-use FDA UDI
Device Name
MICROSTREAM HOOK AND LOOP STRAP , 1 UN FDA UDI
Model / Reference
012604_RMS1 FDA UDI
Description
MICROSTREAM HOOK AND LOOP STRAP , 1 UN FDA UDI

Identifiers

Primary DI / UDI-DI
10884521552289 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

No

FDA UDI
MRI Safety
MR Safe FDA UDI

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

Microstream 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI d1c3b057-b6af-4a88-9c24-5aa425115372 34 fields · synced May 30, 2026