FDA UDI In Commercial Distribution 🇺🇸 United States

Safety Needle

DI: 05907527942064 · Model: 7527942064 · STERIPACK MEDICAL POLAND SP Z O O
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Safety Needle
Primary DI
05907527942064
Version / Model
7527942064
Company Name
STERIPACK MEDICAL POLAND SP Z O O
Labeler DUNS
522155365
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-27
Public Version
1
Public Version Date
2024-03-06
Public Version Status
New
Public Device Record Key
dd7eb33a-1b90-4086-bda3-220e0c1a6f02

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
FMI Needle, Hypodermic, Single Lumen

GMDN Terms

Code Name
59230 Hypodermic needle, single-use

Identifiers

Type ID
Primary 05907527942064