AccessGUDID - DEVICE: MASTER SWIVEL LYNX CLASSIC MOTOR (D8265013503)

GUDID

Device Identifier (DI) Information

Brand Name: MASTER SWIVEL LYNX CLASSIC MOTOR
Version or Model: 5013503
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: MTI Precision Products, LLC

Primary DI Number: D8265013503
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 081600128 *Terms of Use

Device Description: LYNX ETYPE 20000 RPM SWIVEL QUICK DISCONNECT LOW SPEED PNEUMATIC DENTAL MOTOR, USED IN CONJUNCTION WITH OTHER ATTACHMENTS AND CONNECTS TO THE OPERATORY TO DRILL BONE, TEETH AND TOUGH TISSUES IN A DENTAL SETTING.

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?
66228	Dental surgical power tool motor, pneumatic	A hand-held, pneumatically-powered component of a surgical power tool assembly designed to convert the energy from a compressed gas source [e.g., surgical-grade air or nitrogen (N2)] into a non-dedicated mechanical energy for drilling or sawing during dental surgery. It is designed to accept handpiece components/attachments (not included) and is not intended to directly accept an endpiece (e.g., drill bit, saw blade). It might be operated with a hand- or foot-switch. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
EFB	Handpiece, Air-Powered, Dental

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K070001	000

Device Exempt from Premarket Submission: No 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: 263d1f1d-bce4-46d1-a333-f0f93ac89a03
Public Version Date: February 20, 2023
Public Version Number: 1
DI Record Publish Date: February 10, 2023