FDA UDI In Commercial Distribution 🇺🇸 United States

inCourage®

DI: 00841561102747 · Model: 137023-008 · RESPIRATORY TECHNOLOGIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
inCourage®
Primary DI
00841561102747
Version / Model
137023-008
Company Name
RESPIRATORY TECHNOLOGIES, INC.
Labeler DUNS
847990566
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-10
Public Version
4
Public Version Date
2019-12-11
Public Version Status
Update
Public Device Record Key
f0a0505f-7038-48eb-b917-e4dd7f4155be

Device Description

Wrap, XLarge, Northern Lights

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BYI Percussor, Powered-Electric

GMDN Terms

Code Name
38122 Chest-oscillation airway secretion-clearing system vest

Identifiers

Type ID
Primary 00841561102747

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K051383 000

Device Sizes

Type Value Unit Text
Device Size Text, specify XLarge