FDA UDI In Commercial Distribution 🇺🇸 United States

Syntel Silicone Embolectomy Catheter

DI: 00840663109692 · Model: A4F08 · Lemaitre Vascular, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Syntel Silicone Embolectomy Catheter
Primary DI
00840663109692
Version / Model
A4F08
Catalog Number
A4F08
Company Name
Lemaitre Vascular, Inc.
Labeler DUNS
184805166
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-18
Public Version
2
Public Version Date
2022-10-24
Public Version Status
Update
Public Device Record Key
75c36b24-ece7-41e0-b376-be4572d42280

Device Description

Syntel Silicone Embolectomy Catheter - Spring tip

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DXE Catheter, Embolectomy

GMDN Terms

Code Name
58174 Thrombectomy balloon catheter

Identifiers

Type ID
Primary 00840663109692

Customer Contacts

Phone
781-221-2266

Premarket Submissions

Submission Number Supplement Number
K901627 000

Device Sizes

Type Value Unit Text
Catheter Length 80 Centimeter
Catheter Gauge 7 French
Total Volume 2.50 Milliliter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight