FDA UDI In Commercial Distribution 🇺🇸 United States

Precision Xtra

DI: 00093815998778 · Model: 99877 · ABBOTT DIABETES CARE INC
Product Codes
2
GMDN Terms
2
Identifiers
5
Pkg Device Count
100

Basic Information

Brand Name
Precision Xtra
Primary DI
00093815998778
Version / Model
99877
Catalog Number
99877
Company Name
ABBOTT DIABETES CARE INC
Labeler DUNS
966390890
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-07-22
Public Version
7
Public Version Date
2023-10-18
Public Version Status
Update
Public Device Record Key
a30d5c47-7903-4671-95b0-fceb1e4bf472

Device Description

Precision Xtra Blood Glucose Test Strips

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LFR Glucose dehydrogenase, glucose
NBW SYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER

GMDN Terms

Code Name
62643 Multiple clinical chemistry analyte monitoring system IVD, home-use
62644 Multiple clinical chemistry analyte monitoring system IVD, point-of-care

Identifiers

Type ID
Package 30093815998779
Primary 00093815998778
Secondary 57599-9877-5
Unit of Use 10093815998775
Package 40093815998776

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K051213 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
39 – 86 Degrees Fahrenheit