FDA UDI In Commercial Distribution 🇺🇸 United States

GENERATION II VALVED TEARAWAY INTRODUCERGENERATION II VALVED TEARAWAY INTRODUCER

DI: 00884908143423 · Model: DMR191203 · Medical Components, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
GENERATION II VALVED TEARAWAY INTRODUCERGENERATION II VALVED TEARAWAY INTRODUCER
Primary DI
00884908143423
Version / Model
DMR191203
Catalog Number
DMR191203
Company Name
Medical Components, Inc.
Labeler DUNS
038000253
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-12
Public Version
1
Public Version Date
2019-07-22
Public Version Status
New
Public Device Record Key
6362a75a-43bb-407b-8a1e-63d7deef65d0

Device Description

12F (4.1MM ID) X 12CM12F (4.1MM VALVED PEELABLE INTRODUCERVALVED

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
DYB INTRODUCER, CATHETER

GMDN Terms

Code Name
61502 Vascular catheter introduction needle

Identifiers

Type ID
Package 30884908143424
Primary 00884908143423
Package 50884908143428

Customer Contacts