FDA UDI In Commercial Distribution 🇺🇸 United States

TRUEplus

DI: 00021292010805 · Model: TRUEplus 5 bevel Pen Needle 32G/4mm - 100ct box · TRIVIDIA HEALTH, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
TRUEplus
Primary DI
00021292010805
Version / Model
TRUEplus 5 bevel Pen Needle 32G/4mm - 100ct box
Catalog Number
S6H01A32-100
Company Name
TRIVIDIA HEALTH, INC.
Labeler DUNS
151810868
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2018-04-12
Public Version
2
Public Version Date
2018-07-06
Public Version Status
New
Public Device Record Key
eef8e58d-ce56-49d6-bc6c-605e3db97d0d

Device Description

TRUEplus 5 bevel Pen Needle 32G/4mm - 100ct box

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
No
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
44127 Autoinjector needle

Identifiers

Type ID
Package 10021292010802
Primary 00021292010805
Unit of Use 00021292012281

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K171144 000

Device Sizes

Type Value Unit Text
Length 0.16 Inch
Needle Gauge 32 Gauge