FDA UDI In Commercial Distribution 🇺🇸 United States

ULTRAPRO COMFORT PLUG

DI: 10705031228429 · Model: UPLUG403 · Johnson & Johnson International Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ULTRAPRO COMFORT PLUG
Primary DI
10705031228429
Version / Model
UPLUG403
Catalog Number
UPLUG403
Company Name
Johnson & Johnson International Inc.
Labeler DUNS
372587696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-09-24
Public Version
4
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
389492b1-2a03-46b2-b8df-f9c53b18d3f6

Device Description

Partially Absorbable Hernia Repair Device

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
44756 Extra-gynaecological surgical mesh, composite-polymer

Identifiers

Type ID
Package 20705031228426
Primary 10705031228429

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Do not use if package is damaged
Type
Storage Environment Temperature
Temperature Range
High: 30 Degrees Celsius