FDA UDI Not in Commercial Distribution 🇺🇸 United States

Abbott

DI: 00357599000691 · Model: 70901 · ABBOTT DIABETES CARE INC
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
200

Basic Information

Brand Name
Abbott
Primary DI
00357599000691
Version / Model
70901
Catalog Number
70901
Company Name
ABBOTT DIABETES CARE INC
Labeler DUNS
966390890
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2018-06-15
Public Version
3
Public Version Date
2021-01-15
Public Version Status
Update
Public Device Record Key
243021ce-0f42-407f-a2d3-958523fa47b6
Distribution End Date
2021-01-15

Device Description

Abbott SF Single Use Lancing Device

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMK Lancet, blood

GMDN Terms

Code Name
62537 Glucose monitoring system IVD, home-use

Identifiers

Type ID
Package 30357599000692
Primary 00357599000691
Secondary 99073-0709-01
Unit of Use 10357599000698

Customer Contacts