FDA UDI In Commercial Distribution 🇺🇸 United States

VereSee

DI: 00860012249916 · Model: VER-100-102 · Freyja Healthcare, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
VereSee
Primary DI
00860012249916
Version / Model
VER-100-102
Company Name
Freyja Healthcare, LLC
Labeler DUNS
117584088
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-16
Public Version
1
Public Version Date
2025-06-24
Public Version Status
New
Public Device Record Key
478126fc-9640-4b83-aabc-3f7d770327f6

Device Description

VereSee, Optical Veres Needle, Single

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
HIF Insufflator, Laparoscopic

GMDN Terms

Code Name
42412 Laparoscopic access cannula, single-use

Identifiers

Type ID
Primary 00860012249916
Package 00860012249947

Customer Contacts

Phone
833.3739521

Premarket Submissions

Submission Number Supplement Number
K232464 000