FDA UDI In Commercial Distribution 🇺🇸 United States

PROLENE

DI: 10705031050488 · Model: SPMLI · ETHICON, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
PROLENE
Primary DI
10705031050488
Version / Model
SPMLI
Catalog Number
SPMLI
Company Name
ETHICON, LLC
Labeler DUNS
829465157
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-23
Public Version
8
Public Version Date
2025-08-18
Public Version Status
Update
Public Device Record Key
8248afc5-b977-4ac6-993e-0d2ad0ed47a0

Device Description

Soft Polypropylene Mesh, Nonabsorbable Synthetic Surgical 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
60300 Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable

Identifiers

Type ID
Package 20705031050485
Primary 10705031050488

Customer Contacts