AccessGUDID - DEVICE: Aveta Max+ Disposable Resecting Device, 3.9 mm (00850006759729)

GUDID

Device Identifier (DI) Information

Brand Name: Aveta Max+ Disposable Resecting Device, 3.9 mm
Version or Model: 210-2013
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 210-2013
Company Name: MEDITRINA, INC.

Primary DI Number: 00850006759729
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 080570262 *Terms of Use

Device Description: Aveta Max+ Disposable Resecting Device, 3.9 mm, for use with Aveta System

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:	No
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?
46732	Tissue morcellation system handpiece, line-powered	A hand-held component of a tissue morcellation system intended to be used to mechanically cut (slice), core (cut a hole into), peel (remove surface), and extract selected tissue from the body during surgery. It consists of a high-speed rotating blade in a holder and is connected to a line-powered control unit for the transfer of electrical energy or rotational power (via an electrical or remote drive cable); a handpiece obturator, and a disposable remote drive cable may be included. Resected tissue may be removed through suction or manually with a grasping instrument. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HIG	Insufflator, Hysteroscopic
HIH	Hysteroscope (And Accessories)

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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 063204ff-b623-468d-875c-865defb641df
Public Version Date: December 11, 2023
Public Version Number: 1
DI Record Publish Date: December 01, 2023