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Perma Pure

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref ME-060-03-219Model Nafion Dryer, ME Series

by Perma Pure, LLC

Identity

Trade Name
ME-060-03-219 Nafion Dryer EUDAMED
Perma Pure FDA UDI
Generic Name
Gas-sampling/monitoring respiratory tubing, single-use FDA UDI
Device Name
Nafion™ Tube Dryer, ME Series EUDAMED
29" DRYER W/ 51" SL FDA UDI
Model / Reference
Nafion Dryer, ME Series EUDAMED
ME-060-03-219 EUDAMED
ME Series FDA UDI
Description
29" DRYER W/ 51" SL FDA UDI

Identifiers

Catalog Number
ME-060-03-219 FDA UDI
Primary DI / UDI-DI
00840106900633 EUDAMEDFDA UDI
Basic UDI-DI
08401069MESeriesJA EUDAMED
Direct Marketing DI
00840106900633 EUDAMED
FDA Product Code
CBQ FDA UDI
EMDN Code
R9080 RESPIRATORY AND ANESTHESIA DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES EUDAMED
GMDN Term
Gas-sampling/monitoring respiratory tubing, single-use FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
868.1500 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

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

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

Perma Pure by Perma Pure, LLC — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Perma Pure, LLC

Sources (2)

  • FDA UDI 3dd92410-174b-43a3-9aa3-21ede9a36c4f 34 fields · synced Jul 22, 2026
  • EUDAMED e03f3a07-097a-47b3-834f-af8b521d3c83 61 fields · synced Jul 22, 2026