FDA UDI Not in Commercial Distribution 🇺🇸 United States

Dornier MedTech Europe

DI: 01618125160920 · Model: 30415 · TIDI PRODUCTS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Dornier MedTech Europe
Primary DI
01618125160920
Version / Model
30415
Company Name
TIDI PRODUCTS, LLC
Labeler DUNS
063519193
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-12
Public Version
4
Public Version Date
2024-02-05
Public Version Status
Update
Public Device Record Key
9cdfb0b6-bcd4-43ce-b727-208956a2f83d
Distribution End Date
2022-09-21

Device Description

Dornier MedTech Europe Urology Drain Bags Vinyl 32.75in x 26.5in x 1in 20 per Case

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
No
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 01618125160920