FDA UDI In Commercial Distribution 🇺🇸 United States

VanishPoint®

DI: 00613703901392 · Model: 90136 · RETRACTABLE TECHNOLOGIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
500

Basic Information

Brand Name
VanishPoint®
Primary DI
00613703901392
Version / Model
90136
Catalog Number
90136
Company Name
RETRACTABLE TECHNOLOGIES, INC.
Labeler DUNS
838024255
Distribution Status
In Commercial Distribution
Device Count in Pkg
500
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
4285c1b7-e426-4e8f-83aa-583bce9f1823

Device Description

1mL 27G x 1/2" Tuberculin VanishPoint Syringe Bulk Pack Non-Sterile

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
No
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
MEG Syringe, Antistick

GMDN Terms

Code Name
45042 Metered-delivery hypodermic syringe/needle

Identifiers

Type ID
Primary 00613703901392
Unit of Use 00613703901354

Customer Contacts

Phone
888-703-1010

Premarket Submissions

Submission Number Supplement Number
K980069 000