FDA UDI In Commercial Distribution 🇺🇸 United States

Gentrix®

DI: 00386190001554 · Model: PSMT2025 · ACELL, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Gentrix®
Primary DI
00386190001554
Version / Model
PSMT2025
Catalog Number
PSMT2025
Company Name
ACELL, INC.
Labeler DUNS
137258252
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-30
Public Version
11
Public Version Date
2024-02-13
Public Version Status
Update
Public Device Record Key
3ae383d2-6f95-4f26-b934-88672a73156a

Device Description

Gentrix® Surgical Matrix Thick 20 x 25 cm

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

GMDN Terms

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

Identifiers

Type ID
Primary 00386190001554

Customer Contacts

Device Sizes

Type Value Unit Text
Length 25 Centimeter
Width 20 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a clean, dry environment at room temperature