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HME Midi 11

FDA UDI

Class I (US FDA UDI)

by Pharma Systems Ps AB

Identity

Trade Name
HME Midi 11 FDA UDI
Generic Name
Heat/moisture exchanger, single-use FDA UDI
Device Name
HME FDA UDI
Model / Reference
6305 FDA UDI
Description
HME FDA UDI

Identifiers

Catalog Number
6305 FDA UDI
Primary DI / UDI-DI
30734000672226 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 8.5 Centimeter FDA UDI

Category: Heat/moisture exchanger, single-use

HME Midi 11 by Pharma Systems Ps AB — 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

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Manufacturer

Sources (1)

  • FDA UDI 0d667f5d-2761-4985-9f1e-02a16cf25a70 36 fields · synced May 29, 2026