FDA UDI In Commercial Distribution 🇺🇸 United States

Titan

DI: 05701780276979 · Model: 519150 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Titan
Primary DI
05701780276979
Version / Model
519150
Catalog Number
519150
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-11
Public Version
1
Public Version Date
2023-05-19
Public Version Status
New
Public Device Record Key
8e8dd85e-b007-4c11-858e-f29cbe0b15a8

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
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
FHW Device, impotence, mechanical/hydraulic

GMDN Terms

Code Name
36250 Inflatable penile prosthesis

Identifiers

Type ID
Primary 05701780276979

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P000006 064

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from rain. Do not use if package is damaged and consult IFU. Do not resterilize.