AccessGUDID - DEVICE: NA (07613327064841)

GUDID

Device Identifier (DI) Information

Brand Name: NA
Version or Model: 7203000000
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 7203000000
Company Name: STRYKER CORPORATION

Primary DI Number: 07613327064841
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 196548481 *Terms of Use

Device Description: System 7 Single Trigger Rotary Handpiece

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 Names and Definitions: © Copyright GMDN Agency 2015. Reproduced with Permission from the GMDN Agency.

GMDN Preferred Term Name	GMDN Definition
Rechargeable battery-powered surgical power tool system motor	A compact engine that draws power from a rechargeable battery pack intended to convert electrical energy into a non-dedicated mechanical energy to perform a variety of surgical procedures that include drilling, sawing, and inserting involving bones and tough tissues (e.g., cartilage, ligaments). It is typically a pistol-like handpiece that connects to a variety of surgical power tool attachments. The device may be cannulated to permit use of a guidewire. It may be operated with a hand- or foot-switch; it is not intended to draw power from a line-powered control unit. This is a reusable device.

GMDN Preferred Term Name

GMDN Definition

Rechargeable battery-powered surgical power tool system motor

A compact engine that draws power from a rechargeable battery pack intended to convert electrical energy into a non-dedicated mechanical energy to perform a variety of surgical procedures that include drilling, sawing, and inserting involving bones and tough tissues (e.g., cartilage, ligaments). It is typically a pistol-like handpiece that connects to a variety of surgical power tool attachments. The device may be cannulated to permit use of a guidewire. It may be operated with a hand- or foot-switch; it is not intended to draw power from a line-powered control unit. This is a reusable device.

FDA Product Code

[?]

Product Code	Product Code Name
HWE	INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

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
Storage Environment Atmospheric Pressure: between 50 and 106 KiloPascal
Storage Environment Temperature: between -20 and 40 Degrees Celsius
Storage Environment Humidity: between 10 and 75 Percent (%) Relative Humidity

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 3f53ef4f-76ae-44b0-bcb3-f2b95febf443
Public Version Date: March 29, 2018
Public Version Number: 2
DI Record Publish Date: September 24, 2015