FDA UDI Not in Commercial Distribution 🇺🇸 United States

Trilogy

DI: 00606959025394 · Model: Trilogy O2 Ventilator Japan · Respironics, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trilogy
Primary DI
00606959025394
Version / Model
Trilogy O2 Ventilator Japan
Catalog Number
1040004
Company Name
Respironics, Inc.
Labeler DUNS
080728314
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-22
Public Version
6
Public Version Date
2021-03-01
Public Version Status
Update
Public Device Record Key
00e969c1-9ebd-4835-b8f3-e80c4b64c8e7
Distribution End Date
2021-02-28

Device Description

Trilogy O2 Ventilator, Japan

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 00606959025394

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K093905 000

Storage Conditions

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