FDA UDI In Commercial Distribution 🇺🇸 United States

Medpoint

DI: M99204200000BK3 · Model: 1 · Carelife (usa) Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
Medpoint
Primary DI
M99204200000BK3
Version / Model
1
Catalog Number
04-20-0000BK
Company Name
Carelife (usa) Inc.
Labeler DUNS
065756949
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2023-11-01
Public Version
1
Public Version Date
2023-11-09
Public Version Status
New
Public Device Record Key
a336f49c-7a50-45c3-8938-e180fff13539

Device Description

Syringes only 20cc Luer Lock

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
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
FMF Syringe, Piston

GMDN Terms

Code Name
47017 General-purpose syringe, single-use

Identifiers

Type ID
Package M99204200000BK5
Primary M99204200000BK3
Unit of Use M99204200000BK0

Customer Contacts

Phone
7709356499