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Garbin

FDA UDI

Class II (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
Garbin FDA UDI
Generic Name
Portable electric ventilator FDA UDI
Device Name
Garbin Ventilator (Trilogy 100) FDA UDI
Model / Reference
00 FDA UDI
Description
Garbin Ventilator (Trilogy 100) FDA UDI

Identifiers

Catalog Number
1058180 FDA UDI
Primary DI / UDI-DI
00606959022768 FDA UDI
510(k) Number
K083526 FDA UDI
FDA Product Code
DQA FDA UDI
CBK FDA UDI
NOU FDA UDI
GMDN Term
Portable electric ventilator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2700 FDA UDI
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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Portable electric ventilator

Garbin by Respironics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Portable electric ventilator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Respironics, Inc.

Sources (1)

  • FDA UDI 57103b78-f5d0-4e9c-b1be-d1563f170e91 37 fields · synced May 30, 2026