FDA UDI In Commercial Distribution 🇺🇸 United States

PRONOVA

DI: 10705031246140 · Model: PN3526H · ETHICON, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PRONOVA
Primary DI
10705031246140
Version / Model
PN3526H
Catalog Number
PN3526H
Company Name
ETHICON, LLC
Labeler DUNS
829465157
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-28
Public Version
4
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
9c90dd2a-51dc-49d4-81e1-d957cf7e8794

Device Description

Blue Monofilament Poly(Hexafluoropropylene-VDF), Nonabsorbable Surgical Suture

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
GAW SUTURE, NONABSORBABLE, SYNTHETIC, POLYPROPYLENE

GMDN Terms

Code Name
13909 Polyolefin/fluoropolymer suture, monofilament

Identifiers

Type ID
Package 30705031246144
Primary 10705031246140

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K001625 000