AccessGUDID - DEVICE: Oscillating Microsaw G2 (07630055505606)

GUDID

Device Identifier (DI) Information

Brand Name: Oscillating Microsaw G2
Version or Model: 1600657
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: Bien-Air Surgery SA

Primary DI Number: 07630055505606
Issuing Agency: GS1
Commercial Distribution End Date: July 21, 2023
Device Count: 1
Labeler D-U-N-S® Number*: 481597719 *Terms of Use

Device Description: No description.

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:	No
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?
43665	Sawing power tool attachment, oscillating	A device intended to connect to a surgical power tool system motor [it is locked and held in a collet or quick coupling and not simply gripped in a drill chuck (Jacobs chuck)] to convert the non-dedicated mechanical energy provided by the motor to a dedicated mechanical motion to perform an oscillating sawing function when an oscillating saw blade is inserted. This attachment is designed with the cutting teeth arranged in an arc or on a flat plane at its distal end; the teeth are at a 90° angle to its shaft and it cuts when it is moved in a rapid oscillating motion. It is typically made of high-grade stainless steel and synthetic materials and of the macro design. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
DWI	Saw, Electrically Powered

FDA Premarket Submission

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

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

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

Sterilization Method [?]
Moist Heat or Steam Sterilization

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: bb431f7d-a169-4faa-a635-c4de5a47eee4
Public Version Date: July 31, 2023
Public Version Number: 1
DI Record Publish Date: July 21, 2023