FDA UDI In Commercial Distribution 🇺🇸 United States

VanishPoint®

DI: 00613703130105 · Model: 13011 · RETRACTABLE TECHNOLOGIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
VanishPoint®
Primary DI
00613703130105
Version / Model
13011
Catalog Number
13011
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
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
c6f6b6ea-c5a9-4e3d-85aa-19a845aabd75

Device Description

3mL 25G x 1 1/2" VanishPoint® Syringe

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
MEG Syringe, Antistick

GMDN Terms

Code Name
45042 Metered-delivery hypodermic syringe/needle

Identifiers

Type ID
Package 00613703130129
Package 00613703130112
Primary 00613703130105

Customer Contacts

Phone
888-703-1010

Premarket Submissions

Submission Number Supplement Number
K946219 000