FDA UDI In Commercial Distribution 🇺🇸 United States

Insulin Syringe

DI: 00616784695211 · Model: 6952 · DYNAREX CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
10

Basic Information

Brand Name
Insulin Syringe
Primary DI
00616784695211
Version / Model
6952
Company Name
DYNAREX CORPORATION
Labeler DUNS
008124539
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
25d3f0b9-c3fd-4c32-95b9-1a95324434f5

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
No
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
FMF Syringe, Piston

GMDN Terms

Code Name
38501 Insulin syringe/needle, basic

Identifiers

Type ID
Package 00616784695235
Package 00616784695228
Primary 00616784695211
Unit of Use 00616784695204

Premarket Submissions

Submission Number Supplement Number
K112057 000