FDA UDI In Commercial Distribution 🇺🇸 United States

EasyPoint®

DI: 00613703820303 · Model: 82031 · RETRACTABLE TECHNOLOGIES, INC.
Product Codes
1
GMDN Terms
2
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
EasyPoint®
Primary DI
00613703820303
Version / Model
82031
Catalog Number
82031
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
5
Public Version Date
2019-10-23
Public Version Status
Update
Public Device Record Key
975628a1-b46c-44f1-9876-e088b307f448

Device Description

23G x 1" EasyPoint® Needle

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
FMI Needle, Hypodermic, Single Lumen

GMDN Terms

Code Name
17812 Needle guard
59230 Hypodermic needle, single-use

Identifiers

Type ID
Package 00613703820327
Package 00613703820310
Primary 00613703820303

Customer Contacts

Phone
888-703-1010

Premarket Submissions

Submission Number Supplement Number
K133635 000