FDA UDI In Commercial Distribution 🇺🇸 United States

Trilogy

DI: 00606959022720 · Model: Trilogy 202 Ventilator Germany · Respironics, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trilogy
Primary DI
00606959022720
Version / Model
Trilogy 202 Ventilator Germany
Catalog Number
1040003
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
2021-02-15
Public Version Status
Update
Public Device Record Key
02494fbf-4bc1-41a1-89bf-7d8082054930

Device Description

Trilogy 202 Ventilator, German 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
DQA Oximeter
CBK VENTILATOR, CONTINUOUS, FACILITY USE

GMDN Terms

Code Name
47083 Portable electric ventilator

Identifiers

Type ID
Primary 00606959022720

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K093905 000

Storage Conditions

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