FDA UDI In Commercial Distribution 🇺🇸 United States

InoMesh

DI: MDLXMAG120300 · Model: MAG1-2030 · MEDLINX ACACIA PTE. LTD.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
InoMesh
Primary DI
MDLXMAG120300
Version / Model
MAG1-2030
Catalog Number
MAG1-2030
Company Name
MEDLINX ACACIA PTE. LTD.
Labeler DUNS
937305795
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-12-28
Public Version
5
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
8f20a2d2-42b6-4130-83cf-48687c77274d

Device Description

MAG1-2030: 20cm x 30cm (8in x 12in) Mesh Hernia Mesh Polyvinylidene fluoride/Polybutylene adipate

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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
Primary MDLXMAG120300
Package MDLXMAG120303
Package MDLXMAG120302
Package MDLXMAG120301