AccessGUDID - DEVICE: Eclipse Cosmetic Applicator Kit (00853602008215)

GUDID

Device Identifier (DI) Information

Brand Name: Eclipse Cosmetic Applicator Kit
Version or Model: MP1002-CA-K1GF
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: MP1002-CA-K1GF
Company Name: ECLIPSE

Primary DI Number: 00853602008215
Issuing Agency: GS1
Commercial Distribution End Date: May 03, 2019
Device Count: 1
Labeler D-U-N-S® Number*: 969752364 *Terms of Use

Device Description: Cosmetic Applicator Kit with GF (1 CA/pkg) - Includes a sterile, disposable cartridge tip, MicroGlide GF, and a disposable sleeve.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	Yes
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
61222	Cosmetic micro-needling electronic handpiece cartridge, professional	A device intended to be fitted to an electronic cosmetic micro-needling handpiece for the creation of high-density minute skin punctures to stimulate tissue regeneration and improve the appearance of the skin as part of collagen induction therapy (CIT). It is a small, sealed cartridge containing micro-needles intended to be fitted to the distal tip of the handpiece; it does not include any injectable materials. It is intended to be used by a healthcare provider in a clinical setting. It is not intended to be used for energy-based skin treatment. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
No Product Codes

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Storage Environment Temperature: less than 40 Degrees Celsius
Handling Environment Temperature: less than 40 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
Weight: 24.8 Gram
Depth: 1.000 Inch
Width: 2.000 Inch
Height: 4.500 Inch

Device Record Status

Public Device Record Key: f9363c71-f7eb-42a8-a6d8-3c3043df48cd
Public Version Date: November 03, 2023
Public Version Number: 5
DI Record Publish Date: October 04, 2018