FDA UDI In Commercial Distribution 🇺🇸 United States

Paramount

DI: 00618125167395 · Model: 29531 · TIDI PRODUCTS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Paramount
Primary DI
00618125167395
Version / Model
29531
Catalog Number
29531
Company Name
TIDI PRODUCTS, LLC
Labeler DUNS
063519193
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-26
Public Version
3
Public Version Date
2024-02-05
Public Version Status
Update
Public Device Record Key
fe82f3be-e774-4d8a-91e7-7dc6f20cb1a1

Device Description

Paramount Urology Drain Bags Vinyl Fits Hoop Style Urology Frames 50 per Case

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MMZ Table, Cystometric, Electric

GMDN Terms

Code Name
61677 Urological fluid funnel

Identifiers

Type ID
Primary 00618125167395
Previous 01618125167394
Package 10618125167392