FDA UDI In Commercial Distribution 🇺🇸 United States

Precision Xceed Pro

DI: 00357599000257 · Model: 70907-05 · ABBOTT DIABETES CARE INC
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Precision Xceed Pro
Primary DI
00357599000257
Version / Model
70907-05
Catalog Number
70907-05
Company Name
ABBOTT DIABETES CARE INC
Labeler DUNS
966390890
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-26
Public Version
5
Public Version Date
2019-12-11
Public Version Status
Update
Public Device Record Key
adb5f9d2-e1f6-4e2a-821c-f8456d4a53d7

Device Description

Precision Xceed Pro

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
Yes
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
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
JIN NITROPRUSSIDE, KETONES (URINARY, NON-QUANT.)
NBW SYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER
LFR Glucose dehydrogenase, glucose

GMDN Terms

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

Identifiers

Type ID
Primary 00357599000257

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K080960 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-4 – 122 Degrees Fahrenheit