FDA UDI In Commercial Distribution 🇺🇸 United States

Pen Needle

DI: 00369771003390 · Model: 11-305 · GERI-GENTLE CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Pen Needle
Primary DI
00369771003390
Version / Model
11-305
Company Name
GERI-GENTLE CORPORATION
Labeler DUNS
361663839
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-01
Public Version
1
Public Version Date
2023-09-11
Public Version Status
New
Public Device Record Key
2867576c-1005-46ea-a9be-c68a923f40e9

Device Description

Safety Pen Needle 30G

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMI Needle, Hypodermic, Single Lumen

GMDN Terms

Code Name
17180 Subcutaneous infusion/injection port needle

Identifiers

Type ID
Primary 00369771003390
Package 00369771003406

Premarket Submissions

Submission Number Supplement Number
K192677 000