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Dustfilter 40pcs Reus.Abso.Flow-i

FDA UDI

Class I (US FDA UDI)

by Maquet Critical Care AB

Identity

Trade Name
Dustfilter 40pcs Reus.Abso.Flow-i FDA UDI
Generic Name
Anaesthesia workstation, general-purpose FDA UDI
Device Name
Contains 2x20 pc of filter without direct marking FDA UDI
Model / Reference
6880430 FDA UDI
Description
Contains 2x20 pc of filter without direct marking FDA UDI

Identifiers

Primary DI / UDI-DI
17325710000998 FDA UDI
FDA Product Code
BSF FDA UDI
GMDN Term
Anaesthesia workstation, general-purpose FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5310 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

No

FDA UDI

Category: Anaesthesia workstation, general-purpose

Dustfilter 40pcs Reus.Abso.Flow-i by Maquet Critical Care AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia workstation, general-purpose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Maquet Critical Care AB

Sources (1)

  • FDA UDI c74a44c1-8efc-4c73-9a86-014a5c21da54 33 fields · synced Jun 8, 2026