FDA UDI In Commercial Distribution 🇺🇸 United States

Diagnostix™

DI: 00634782063030 · Model: 2100-2BK · AMERICAN DIAGNOSTIC CORP
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Diagnostix™
Primary DI
00634782063030
Version / Model
2100-2BK
Catalog Number
2100-2BK
Company Name
AMERICAN DIAGNOSTIC CORP
Labeler DUNS
108999095
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
5
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
2cc908d5-ed6d-48af-89e3-58abe0f1c772

Device Description

Rubber Bumper, Pulse Ox,Black

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
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
45607 Pulse oximeter

Identifiers

Type ID
Package 00634782562847
Package 00634782862848
Primary 00634782063030

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K101577 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
14 – 104 Degrees Fahrenheit
Type
Storage Environment Humidity
Temperature Range
10 – 80 Percent (%) Relative Humidity