FDA UDI In Commercial Distribution 🇺🇸 United States

Nix

DI: 00363736109387 · Model: 10363736109384 · Medtech Products Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Nix
Primary DI
00363736109387
Version / Model
10363736109384
Company Name
Medtech Products Inc.
Labeler DUNS
060272465
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-24
Public Version
2
Public Version Date
2023-07-03
Public Version Status
Update
Public Device Record Key
4549e2c8-5c76-4977-a2d7-2eb2f8e96f08

Device Description

Nix Ultra 3.4 oz Liquid

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LIL Monitor, Penile Tumescence

GMDN Terms

Code Name
45370 Lice removal/prevention kit

Identifiers

Type ID
Primary 00363736109387
Package 10363736111929

Customer Contacts