FDA UDI In Commercial Distribution 🇺🇸 United States

DiaDoc

DI: 00860010611210 · Model: 30G 1cc 12.7mm · INSULIFE LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
DiaDoc
Primary DI
00860010611210
Version / Model
30G 1cc 12.7mm
Company Name
INSULIFE LLC
Labeler DUNS
125286574
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2023-09-09
Public Version
1
Public Version Date
2023-09-18
Public Version Status
New
Public Device Record Key
45096705-0fac-4bbf-9751-eda660ebb585

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
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
FMF Syringe, Piston

GMDN Terms

Code Name
38501 Insulin syringe/needle, basic

Identifiers

Type ID
Unit of Use 10860010611217
Primary 00860010611210