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Perma Pure

FDA UDI

Class II (US FDA UDI)

by Perma Pure, LLC

Identity

Trade Name
PERMA PURE FDA UDI
Generic Name
Gas-sampling/monitoring respiratory tubing, single-use FDA UDI
Device Name
ME-070-03-24 36" ME with Male Luers FDA UDI
Model / Reference
ME Series FDA UDI
Description
ME-070-03-24 36" ME with Male Luers FDA UDI

Identifiers

Catalog Number
ME-070-03-24 FDA UDI
Primary DI / UDI-DI
00840106906086 FDA UDI
FDA Product Code
CBQ FDA UDI
GMDN Term
Gas-sampling/monitoring respiratory tubing, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1500 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

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

Perma Pure by Perma Pure, LLC — 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

Manufacturer
Perma Pure, LLC

Sources (1)

  • FDA UDI bcff1edc-07f8-4dd4-a189-7fb490cb8cfd 34 fields · synced Jun 8, 2026