AccessGUDID - DEVICE: Carbon offset reamer handle Hudson dual coupling (07640187914023)

GUDID

Device Identifier (DI) Information

Brand Name: Carbon offset reamer handle Hudson dual coupling
Version or Model: T17876
Commercial Distribution Status: In Commercial Distribution
Catalog Number: T17876
Company Name: MPS Micro Precision Systems AG

Primary DI Number: 07640187914023
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 482204059 *Terms of Use

Device Description: Offset Reamer handles designed for required minimally invasive surgical approach of the hip joint. A non clipped and dual connection with reamer cutting tool and 3 couplings with power tool (Big AO, Stryker-Zimmer/Hall and Hudson) are available. It could be disassembled in 5 parts allowing the cleaning of the instrument. This is a reusable device.

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?
47845	Surgical power tool adaptor	A connecting device designed as a mechanical coupling to join and lock together a distal tool to the surgical power tool to provide the power when these are incompatible and are of a different manufacture/industry standard. It is typically made from high-grade stainless steel and/or synthetic material and is available in a variety of shapes and sizes. This device may be cannulated to allow the use of a guidewire. There are various types such as a Hudson adaptor, Trinkle adaptor, Zimmer adaptor. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LXH	Orthopedic Manual Surgical Instrument

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: f4556057-7c49-4b8e-820d-d30b9d524e15
Public Version Date: November 18, 2022
Public Version Number: 2
DI Record Publish Date: August 13, 2020