FDA UDI In Commercial Distribution 🇺🇸 United States

Medtfine

DI: M992304031803 · Model: 1 · Carelife (usa) Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Medtfine
Primary DI
M992304031803
Version / Model
1
Catalog Number
30-40-3180
Company Name
Carelife (usa) Inc.
Labeler DUNS
065756949
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2017-02-11
Public Version
6
Public Version Date
2023-02-17
Public Version Status
Update
Public Device Record Key
512c816f-baa5-4164-8001-d17eaa2d5f5e

Device Description

Pen Needles 31G*8mm

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
44127 Autoinjector needle

Identifiers

Type ID
Primary M992304031803
Unit of Use M992304031800
Package M992304031805

Customer Contacts

Phone
7709356499

Device Sizes

Type Value Unit Text
Needle Gauge 31 Gauge