FDA UDI In Commercial Distribution 🇺🇸 United States

Sundt™

DI: 10381780211129 · Model: NL8505063 · Integra Lifesciences Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Sundt™
Primary DI
10381780211129
Version / Model
NL8505063
Catalog Number
NL8505063
Company Name
Integra Lifesciences Corporation
Labeler DUNS
083171244
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-20
Public Version
5
Public Version Date
2023-05-15
Public Version Status
Update
Public Device Record Key
5b7ab142-bdf2-40bd-b41b-540e12c75d62

Device Description

Sundt™ Internal Carotid Endarterectomy Shunt

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
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
DWF CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS

GMDN Terms

Code Name
47113 Carotid artery shunt

Identifiers

Type ID
Secondary M269NL85050631
Primary 10381780211129

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 3.5mm x 4mm; Distal Tubing: 2mm I.D x 3.5mm O.D.; Proximal Tubing: 2mm x 4mm O.D.; Total Length: 10cm