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Aeroneb Module Solo kit, SERVO-i

FDA UDI

Class II (US FDA UDI)

by Maquet Critical Care AB

Identity

Trade Name
Aeroneb Module Solo kit, SERVO-i FDA UDI
Generic Name
Neonatal/adult intensive-care ventilator FDA UDI
Device Name
Following Device Identifier numbers are included in this KIT: 07325710002841, 07325710004807 FDA UDI
Model / Reference
6685347 FDA UDI
Description
Following Device Identifier numbers are included in this KIT: 07325710002841, 07325710004807 FDA UDI

Identifiers

Primary DI / UDI-DI
07325710001561 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

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

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

Aeroneb Module Solo kit, SERVO-i 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 cb5cdcd8-ef67-4b9f-a607-abb92bd6b70c 33 fields · synced Jun 1, 2026