FDA UDI In Commercial Distribution 🇺🇸 United States

Drive

DI: 00822383259758 · Model: 18720 · Drive Devilbiss Healthcare
Product Codes
1
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Drive
Primary DI
00822383259758
Version / Model
18720
Company Name
Drive Devilbiss Healthcare
Labeler DUNS
867673159
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
4
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
90e7fe73-d30c-42b8-9f18-a25de784eb78

Device Description

Digital Handy-Ox

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

GMDN Terms

Code Name
17667 Telemetric pulse oximeter
45607 Pulse oximeter

Identifiers

Type ID
Package 10822383259755
Primary 00822383259758

Premarket Submissions

Submission Number Supplement Number
K090671 000