← Back to catalogue

Procure

FDA UDI

Class I (US FDA UDI)

by Twin Med, LLC

Identity

Trade Name
Procure FDA UDI
Generic Name
Heat/moisture exchanger, single-use FDA UDI
Device Name
HMEF Straight Small W/Sampling Port 150 - 1500 VT Range 35.3 ml Dead Space FDA UDI
Model / Reference
1002218 FDA UDI
Description
HMEF Straight Small W/Sampling Port 150 - 1500 VT Range 35.3 ml Dead Space FDA UDI

Identifiers

Catalog Number
1002218 FDA UDI
Primary DI / UDI-DI
10840330700181 FDA UDI
FDA Product Code
BYD FDA UDI
GMDN Term
Heat/moisture exchanger, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5375 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Heat/moisture exchanger, single-use

Procure by Twin Med, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Heat/moisture exchanger, 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

Manufacturer
Twin Med, LLC

Sources (1)

  • FDA UDI 819685ce-aabf-4f02-a72d-8eb3dbbf1085 35 fields · synced May 30, 2026