FDA UDI In Commercial Distribution 🇺🇸 United States

exGraft

DI: 00818136020010 · Model: RGX062501 · PECA LABS, INC.
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
exGraft
Primary DI
00818136020010
Version / Model
RGX062501
Catalog Number
RUX062501
Company Name
PECA LABS, INC.
Labeler DUNS
078340058
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-04
Public Version
3
Public Version Date
2025-12-25
Public Version Status
Update
Public Device Record Key
c2b5e43a-63ad-4845-8c20-1705338b8474

Device Description

6mm ID X 25cm Length exGraft ePTFE Vascular Graft

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
Yes
MRI Safety
MR Conditional
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
DYF Prosthesis, Vascular Graft, Of Less Then 6mm Diameter

GMDN Terms

Code Name
35281 Synthetic vascular graft, non-medicated

Identifiers

Type ID
Package 00818136020539
Primary 00818136020010

Device Sizes

Type Value Unit Text
Length 25 Centimeter
Lumen/Inner Diameter 6 Millimeter