FDA UDI In Commercial Distribution 🇺🇸 United States

Gelweave™

DI: 05037881998190 · Model: 733042 · VASCUTEK LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Gelweave™
Primary DI
05037881998190
Version / Model
733042
Catalog Number
733042
Company Name
VASCUTEK LTD
Labeler DUNS
229053087
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-19
Public Version
7
Public Version Date
2022-10-03
Public Version Status
Update
Public Device Record Key
6c4a1181-5218-4e12-9f25-d4202af23533

Device Description

Gelweave Gelatin Impregnated Woven Vascular Prosthesis LARGE BORE GELWEAVE

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
Labeling does not contain MRI Safety Information
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
DSY PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER

GMDN Terms

Code Name
35281 Synthetic vascular graft

Identifiers

Type ID
Primary 05037881998190

Customer Contacts

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 42 Millimeter
Length 30 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in clean, dry area at room temperature. The prosthesis must be implanted within one month after removal from the foil pouch.