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Gas cylinder Restrainer Servo-s

FDA UDI

Class II (US FDA UDI)

by Maquet Critical Care AB

Identity

Trade Name
Gas cylinder Restrainer Servo-s FDA UDI
Generic Name
Neonatal/adult intensive-care ventilator FDA UDI
Device Name
Following Device Identifier is including in this KIT: 07325710003152 FDA UDI
Model / Reference
6650514 FDA UDI
Description
Following Device Identifier is including in this KIT: 07325710003152 FDA UDI

Identifiers

Primary DI / UDI-DI
07325710000588 FDA UDI
FDA Product Code
CBK FDA UDI
GMDN Term
Neonatal/adult intensive-care ventilator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5895 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

Yes

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: Neonatal/adult intensive-care ventilator

Gas cylinder Restrainer Servo-s by Maquet Critical Care AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neonatal/adult intensive-care ventilator.

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 3549c358-2923-4137-98d0-e46b7b89909f 33 fields · synced May 30, 2026