FDA UDI In Commercial Distribution 🇺🇸 United States

KETO-DIASTIX®

DI: 10301932883509 · Model: 2883 · ASCENSIA DIABETES CARE US INC.
Product Codes
2
GMDN Terms
1
Identifiers
5
Pkg Device Count
50

Basic Information

Brand Name
KETO-DIASTIX®
Primary DI
10301932883509
Version / Model
2883
Catalog Number
2883
Company Name
ASCENSIA DIABETES CARE US INC.
Labeler DUNS
080028910
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2019-06-06
Public Version
4
Public Version Date
2022-11-28
Public Version Status
Update
Public Device Record Key
4ca9ef20-05e0-4e9f-af3f-7c22ec312b1f

Device Description

Reagent Strips for Urinalysis: Ketone; Glucose

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
JIL Method, Enzymatic, Glucose (Urinary, Non-Quantitative)
JIN Nitroprusside, Ketones (Urinary, Non-Quant.)

GMDN Terms

Code Name
54514 Multiple urine analyte IVD, kit, rapid colorimetric, clinical

Identifiers

Type ID
Package 40301932883500
Package 00301932883502
Primary 10301932883509
Secondary 0193-2882-50
Unit of Use 00301932883014

Customer Contacts

Phone
800-348-8100

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store out of direct sunlight. Replace cap immediately and tightly. Do not remove desiccant from bottle. Read enclosed directions carefully. Use within 6 mos after first open. Tamper evident seal.
Type
Storage Environment Temperature
Temperature Range
59 – 86 Degrees Fahrenheit