FDA UDI In Commercial Distribution 🇺🇸 United States

TIDI

DI: 00618125141128 · Model: 5313 N/S · TIDI PRODUCTS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
TIDI
Primary DI
00618125141128
Version / Model
5313 N/S
Catalog Number
5313 N/S
Company Name
TIDI PRODUCTS, LLC
Labeler DUNS
063519193
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-28
Public Version
3
Public Version Date
2024-02-08
Public Version Status
Update
Public Device Record Key
96c5d0c1-198a-406e-8156-46cb308a7a11

Device Description

Uro-Catcher Bag

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
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
Package 10618125141125
Primary 00618125141128
Previous 01618125141127