FDA UDI In Commercial Distribution 🇺🇸 United States

Restorelle

DI: 05708932484022 · Model: 501450 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Restorelle
Primary DI
05708932484022
Version / Model
501450
Catalog Number
501450
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-22
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
d61795c9-f3a2-4b0f-915d-43f53c817d2b

Device Description

Direct Fix™ Anterior Polypropylene Mesh

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
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
FTL Mesh, surgical, polymeric

GMDN Terms

Code Name
60842 Pelvic organ prolapse surgical mesh, synthetic polymer

Identifiers

Type ID
Primary 05708932484022

Customer Contacts

Device Sizes

Type Value Unit Text
Width 11 Centimeter
Length 16 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep out of sunlight