FDA UDI In Commercial Distribution 🇺🇸 United States

MediMax Tech

DI: 00817325023498 · Model: SPEC · MEDIMAX TECH INC.
Product Codes
1
GMDN Terms
2
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
MediMax Tech
Primary DI
00817325023498
Version / Model
SPEC
Company Name
MEDIMAX TECH INC.
Labeler DUNS
927071162
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-02-21
Public Version
2
Public Version Date
2020-08-11
Public Version Status
Update
Public Device Record Key
19adaf21-ef23-47df-9444-28561f15f879

Device Description

EvaQMaxPen, Smoke Pencil, Eco, Button, Holster, Non-Stick Blade, 3 Meter Hose - Each

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
Yes
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
37861 Surgical plume evacuation system
61870 Open-surgery electrosurgical handpiece/electrode, monopolar, reusable

Identifiers

Type ID
Primary 00817325023498
Package 10817325023495
Package 20817325023492
Package 30817325023499

Customer Contacts

Phone
855-633-4629

Premarket Submissions

Submission Number Supplement Number
K092732 000
K143103 000