FDA UDI In Commercial Distribution 🇺🇸 United States

Trilogy

DI: 00606959026230 · Model: Trilogy 200 Ventilator, U.S.A.-Recert · Respironics, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trilogy
Primary DI
00606959026230
Version / Model
Trilogy 200 Ventilator, U.S.A.-Recert
Catalog Number
U1040005
Company Name
Respironics, Inc.
Labeler DUNS
080728314
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-23
Public Version
5
Public Version Date
2021-02-22
Public Version Status
Update
Public Device Record Key
50f64b5f-b639-4c31-aa8b-679e7d34db97

Device Description

Trilogy 200 Ventilator Recertified, U.S.A version

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
CBK VENTILATOR, CONTINUOUS, FACILITY USE
DQA Oximeter

GMDN Terms

Code Name
47083 Portable electric ventilator

Identifiers

Type ID
Primary 00606959026230

Customer Contacts

Storage Conditions

Type
Handling Environment Humidity
Temperature Range
15 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-20 – 60 Degrees Celsius