FDA UDI In Commercial Distribution 🇺🇸 United States

Duramesh

DI: 00850008298134 · Model: MSI-501 · Mesh Suture Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Duramesh
Primary DI
00850008298134
Version / Model
MSI-501
Company Name
Mesh Suture Inc.
Labeler DUNS
116375032
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-31
Public Version
1
Public Version Date
2023-09-08
Public Version Status
New
Public Device Record Key
029da697-ce31-4e05-aa7a-4773ff6779ef

Device Description

DURAMESH™ 2 Mesh Suture: Large Needle – USA

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
GAW Suture, Nonabsorbable, Synthetic, Polypropylene

GMDN Terms

Code Name
13907 Polyolefin/fluoropolymer suture, multifilament

Identifiers

Type ID
Package 10850008298131
Primary 00850008298134

Customer Contacts

Phone
800-298-5468

Premarket Submissions

Submission Number Supplement Number
K211178 000