FDA UDI In Commercial Distribution 🇺🇸 United States

VACUTEST KIMA S.R.L.

DI: 18053848993019 · Model: 15193 · MEUS SRL
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
100

Basic Information

Brand Name
VACUTEST KIMA S.R.L.
Primary DI
18053848993019
Version / Model
15193
Catalog Number
15193
Company Name
MEUS SRL
Labeler DUNS
514346550
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2023-09-06
Public Version
1
Public Version Date
2023-09-14
Public Version Status
New
Public Device Record Key
7fdb4435-78ce-495a-9440-b677797dc74b

Device Description

STERILE MULTI-SAMPLE NEEDLES 18 G X 1" W/DROP PROOF RUBBER-PINK

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
35209 Non-fixed blood collection needle

Identifiers

Type ID
Package 28053848993016
Primary 18053848993019
Package 38053848993013
Unit of Use 08053848993012

Customer Contacts

Device Sizes

Type Value Unit Text
Needle Gauge 18 Gauge

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 25 Degrees Celsius