FDA UDI In Commercial Distribution 🇺🇸 United States

ULTRAPRO

DI: 10705031132597 · Model: UPPM6 · Johnson & Johnson International Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ULTRAPRO
Primary DI
10705031132597
Version / Model
UPPM6
Catalog Number
UPPM6
Company Name
Johnson & Johnson International Inc.
Labeler DUNS
372587696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-01
Public Version
7
Public Version Date
2022-12-29
Public Version Status
Update
Public Device Record Key
4a0411e5-8e23-4d13-bdf9-2cf1faab6738

Device Description

Polypropylene partially absorbable medium blue / undyed Plug and Onlay Patch

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
MR Safe
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 20705031132594
Primary 10705031132597

Customer Contacts