FDA UDI In Commercial Distribution 🇺🇸 United States

VanishPoint®

DI: 00613703241306 · Model: 24131 · RETRACTABLE TECHNOLOGIES, INC.
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
VanishPoint®
Primary DI
00613703241306
Version / Model
24131
Catalog Number
24131
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
2021-04-07
Public Version Status
Update
Public Device Record Key
cfed7e59-a576-499b-8c50-73a099074f23

Device Description

21G x 3/4" w/12" tubing VanishPoint® Blood Collection Set

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
FPA Set, Administration, Intravascular
JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

GMDN Terms

Code Name
58497 Blood collection set, invasive

Identifiers

Type ID
Package 00613703241320
Package 00613703241313
Primary 00613703241306

Customer Contacts

Phone
888-703-1010