FDA UDI In Commercial Distribution 🇺🇸 United States

VanishPoint®

DI: 00613703353306 · Model: 35331 · RETRACTABLE TECHNOLOGIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
VanishPoint®
Primary DI
00613703353306
Version / Model
35331
Catalog Number
35331
Company Name
RETRACTABLE TECHNOLOGIES, INC.
Labeler DUNS
838024255
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-22
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
40fc70c7-6181-4b80-a4a3-5c4c26fce76b

Device Description

22G x 1" VanishPoint® IV Catheter FEP

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
FOZ Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days

GMDN Terms

Code Name
40601 Peripheral vascular catheter

Identifiers

Type ID
Package 00613703353320
Package 00613703353313
Primary 00613703353306

Customer Contacts

Phone
888-703-1010