FDA UDI In Commercial Distribution 🇺🇸 United States

LimFlow V-Ceiver

DI: 00850041730004 · Model: VC-US-21 · Limflow Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LimFlow V-Ceiver
Primary DI
00850041730004
Version / Model
VC-US-21
Company Name
Limflow Inc.
Labeler DUNS
096651686
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-26
Public Version
2
Public Version Date
2023-09-21
Public Version Status
Update
Public Device Record Key
7674acbf-ee7c-4a46-925f-3610442c3baf

Device Description

The LimFlow V-Ceiver is intended for use in the cardiovascular system to manipulate and retrieve guidewires specified in the IFU.

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
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
MMX Device, Percutaneous Retrieval

GMDN Terms

Code Name
17927 Intravascular extraction catheter-snare

Identifiers

Type ID
Primary 00850041730004

Customer Contacts

Phone
18884787705

Premarket Submissions

Submission Number Supplement Number
K222083 000