AccessGUDID - DEVICE: MECTRON (E322029001150010)

GUDID

Device Identifier (DI) Information

Brand Name: MECTRON
Version or Model: PS MEDICAL L TORQUE WRENCH
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 02900115-001
Company Name: MECTRON SPA

Primary DI Number: E322029001150010
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 436664734 *Terms of Use

Device Description: PS MEDICAL L TORQUE WRENCH is a torque wrench that allows to secure the extension of long inserts to the Mectron ultrasonic handpieces.

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?
47675	Ultrasonic surgical system torque wrench, reusable	A hand-held instrument designed to manually attach or detach a handpiece tip (blade) from the handpiece of an ultrasonic surgical system. It is typically formed with a socket that is placed over the handpiece tip and rotated by the operator to tighten or loosen, with appropriate torque, the tip to or from the handpiece. The device is made of durable materials and typically includes a mechanism to prevent under- or over-tightening. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HWE	Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
HBE	Drills, Burrs, Trephines & Accessories (Simple, Powered)
ERL	Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
JDX	Instrument, Surgical, Sonic And Accessory/Attachment
DZI	Drill, Bone, Powered

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K153743	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: 401849fd-0ee2-4bf3-b110-e3113aafedec
Public Version Date: July 06, 2018
Public Version Number: 3
DI Record Publish Date: August 30, 2016