FDA UDI In Commercial Distribution 🇺🇸 United States

Starplex

DI: 00840165400877 · Model: V102-POUCH · Pretium Canada Packaging ULC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Starplex
Primary DI
00840165400877
Version / Model
V102-POUCH
Company Name
Pretium Canada Packaging ULC
Labeler DUNS
246665038
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2025-02-21
Public Version
1
Public Version Date
2025-03-03
Public Version Status
New
Public Device Record Key
8f1044f2-aef7-4b0e-b668-26bce328fef9

Device Description

10 ml Vial with White Cap, Individually Peel Packed, 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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMH Container, Specimen, Sterile

GMDN Terms

Code Name
47775 General specimen container IVD, no additive/medium

Identifiers

Type ID
Unit of Use 10840165400874
Primary 00840165400877