FDA UDI In Commercial Distribution 🇺🇸 United States

Veress Needle

DI: 04714127862026 · Model: FVN115000 · UNIMAX MEDICAL SYSTEMS INC.
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Veress Needle
Primary DI
04714127862026
Version / Model
FVN115000
Company Name
UNIMAX MEDICAL SYSTEMS INC.
Labeler DUNS
658122465
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-19
Public Version
4
Public Version Date
2020-07-14
Public Version Status
Update
Public Device Record Key
0231f24d-ce51-44bb-80b8-6ad0740640b9

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
HIF Insufflator, Laparoscopic
FHO Pneumoperitoneum Needle

GMDN Terms

Code Name
12750 Spring-loaded pneumoperitoneum needle, single-use

Identifiers

Type ID
Package 24714127862020
Package 14714127862023
Primary 04714127862026

Premarket Submissions

Submission Number Supplement Number
K111441 000

Device Sizes

Type Value Unit Text
Length 15 Centimeter