← Back to catalogue

Reusable Absorber

FDA UDI

Class I (US FDA UDI)

by Maquet Critical Care AB

Identity

Trade Name
Reusable Absorber FDA UDI
Generic Name
Anaesthesia workstation, general-purpose FDA UDI
Model / Reference
6692582 FDA UDI

Identifiers

Primary DI / UDI-DI
07325710002872 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

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

Reusable Absorber 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 8dabfd38-3f2d-41c5-8bee-366831d72ba0 32 fields · synced May 30, 2026