FDA UDI In Commercial Distribution 🇺🇸 United States

Marketlab Inc

DI: 00817517020816 · Model: 43569 · MARKETLAB INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Marketlab Inc
Primary DI
00817517020816
Version / Model
43569
Catalog Number
43569
Company Name
MARKETLAB INC.
Labeler DUNS
848917027
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-16
Public Version
1
Public Version Date
2018-12-17
Public Version Status
New
Public Device Record Key
53dcb19f-0c5f-4f9a-8fb1-a8f3abd778fd

Device Description

23-Gauge Shot Prep Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
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
47017 General-purpose syringe, single-use

Identifiers

Type ID
Primary 00817517020816
Package 00817517020823

Customer Contacts