FDA UDI In Commercial Distribution 🇺🇸 United States

STERiJECT TM

DI: 14580708061808 · Model: HPC-25025A · TSK LABORATORY, JAPAN
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
STERiJECT TM
Primary DI
14580708061808
Version / Model
HPC-25025A
Company Name
TSK LABORATORY, JAPAN
Labeler DUNS
690646096
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2023-05-30
Public Version
1
Public Version Date
2023-06-07
Public Version Status
New
Public Device Record Key
5d1117b6-8b65-4ee6-bc74-962d8ef8b1c4

Device Description

TSK STERiJECT Premium Disposable Hypodermic Needle

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
Yes
Has Expiration Date
Yes
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
59230 Hypodermic needle, single-use

Identifiers

Type ID
Package 24580708061805
Primary 14580708061808
Unit of Use 04571225313672

Premarket Submissions

Submission Number Supplement Number
K970370 000

Device Sizes

Type Value Unit Text
Outer Diameter 0.5 Millimeter
Length 25 Millimeter