FDA UDI In Commercial Distribution 🇺🇸 United States

KETOSTIX®

DI: 10301932880508 · Model: 2880 · ASCENSIA DIABETES CARE US INC.
Product Codes
1
GMDN Terms
1
Identifiers
5
Pkg Device Count
50

Basic Information

Brand Name
KETOSTIX®
Primary DI
10301932880508
Version / Model
2880
Catalog Number
2880
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
3
Public Version Date
2022-11-28
Public Version Status
Update
Public Device Record Key
204206dc-dee1-4faf-8a34-e74764f325a9

Device Description

Reagent Strips for Urinalysis: Ketone

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
JIN Nitroprusside, Ketones (Urinary, Non-Quant.)

GMDN Terms

Code Name
54519 Urine ketone IVD, kit, rapid colorimetric, clinical

Identifiers

Type ID
Package 40301932880509
Package 00301932880501
Primary 10301932880508
Secondary 0193-2880-50
Unit of Use 00301932880013

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