FDA UDI Not in Commercial Distribution 🇺🇸 United States

Gentrix®

DI: 00386190001523 · Model: PSMT1020 · ACELL, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Gentrix®
Primary DI
00386190001523
Version / Model
PSMT1020
Catalog Number
PSMT1020
Company Name
ACELL, INC.
Labeler DUNS
137258252
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-30
Public Version
9
Public Version Date
2023-10-04
Public Version Status
Update
Public Device Record Key
a2fb9135-0c28-48ab-8db3-757f09153aa1
Distribution End Date
2020-06-05

Device Description

Surgical Matrix Thick 10 x 20 cm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OXK Mesh, surgical, collagen, large abdominal wall defects
OXH Mesh, surgical, collagen, plastic and reconstructive surgery
FTM Mesh, surgical

GMDN Terms

Code Name
60907 Extra-gynaecological surgical mesh, collagen, bioabsorbable, non-antimicrobial

Identifiers

Type ID
Primary 00386190001523

Customer Contacts

Device Sizes

Type Value Unit Text
Length 20 Centimeter
Width 10 Centimeter