FDA UDI In Commercial Distribution 🇺🇸 United States

ULTRAPRO

DI: 10705031132399 · Model: UML1 · Johnson & Johnson International Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ULTRAPRO
Primary DI
10705031132399
Version / Model
UML1
Catalog Number
UML1
Company Name
Johnson & Johnson International Inc.
Labeler DUNS
372587696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-21
Public Version
6
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
3100127a-bb5e-4884-8153-1bf6f7460c94

Device Description

Ultrapro MONOCRYL™-PROLENE™- COMPOSITE Poliglecaprone 25/Polypropylene Sterile, Synthetic, Partially Absorbable 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
44756 Extra-gynaecological surgical mesh, composite-polymer

Identifiers

Type ID
Primary 10705031132399

Customer Contacts