FDA UDI In Commercial Distribution 🇺🇸 United States

Compound W®

DI: 00075137000032 · Model: CWUS004502, CWUS004103, CWUS004602 · Medtech Products Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Compound W®
Primary DI
00075137000032
Version / Model
CWUS004502, CWUS004103, CWUS004602
Catalog Number
N/A
Company Name
Medtech Products Inc.
Labeler DUNS
060272465
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-16
Public Version
2
Public Version Date
2023-07-03
Public Version Status
Update
Public Device Record Key
fcd4641a-9553-4e3a-b9e2-7b1bd4324484

Device Description

Compound W® Nitrofreeze™ Nitrous Oxide Wart Removal System

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
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
No
Sterilization Prior Use
No

Product Codes

Code Name
GEH Unit, Cryosurgical, Accessories

GMDN Terms

Code Name
42518 Wart-removal cryogenic kit

Identifiers

Type ID
Primary 00075137000032
Package 10075137000039

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Protect from sunlight Do not expose to temps above 50C(100F) before first use or 35C(95F) after 1st use. Exposure to temps >35C(95F) will activate safety feature disabling the device. Store @room temp