FDA UDI In Commercial Distribution 🇺🇸 United States

EndyMed Intensif 10 Tips Package

DI: 07290016814323 · Model: Intensif 10 Tips Package · ENDYMED MEDICAL LTD
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EndyMed Intensif 10 Tips Package
Primary DI
07290016814323
Version / Model
Intensif 10 Tips Package
Catalog Number
ND_PRD00045
Company Name
ENDYMED MEDICAL LTD
Labeler DUNS
531958689
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-31
Public Version
3
Public Version Date
2023-11-21
Public Version Status
Update
Public Device Record Key
3936b940-6957-4669-b3bd-c0914c8f8513

Device Description

Tips that are used with the intensif handpiece (1st generation).

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
No
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
OUH Skin Resurfacing Rf Applicator

GMDN Terms

Code Name
61222 Cosmetic micro-needling electronic handpiece cartridge, professional

Identifiers

Type ID
Primary 07290016814323

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K130501 000