FDA UDI Not in Commercial Distribution 🇺🇸 United States

Trilogy

DI: 00606959025370 · Model: Trilogy200 Ventilator, Japan · Respironics, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trilogy
Primary DI
00606959025370
Version / Model
Trilogy200 Ventilator, Japan
Catalog Number
1032804
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
5
Public Version Date
2021-03-01
Public Version Status
Update
Public Device Record Key
a34f8636-e8db-4f43-be97-568b4ed93144
Distribution End Date
2021-02-28

Device Description

Trilogy 200 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
DQA Oximeter
CBK VENTILATOR, CONTINUOUS, FACILITY USE

GMDN Terms

Code Name
47083 Portable electric ventilator

Identifiers

Type ID
Primary 00606959025370

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K093416 000

Storage Conditions

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