AccessGUDID - DEVICE: V. Mueller (10885403009518)

GUDID

Device Identifier (DI) Information

Brand Name: V. Mueller
Version or Model: AU11360
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: AU11360
Company Name: CAREFUSION 2200, INC

Primary DI Number: 10885403009518
Issuing Agency: GS1
Commercial Distribution End Date: February 11, 2019
Device Count: 1
Labeler D-U-N-S® Number*: 832696038 *Terms of Use

Device Description: LEMPERT MALLEUS CUTTER JAW LENGTH 11MM OVERALL LENGTH 4-1/2" (11.4CM)

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?
35213	Middle ear malleus nipper	A hand-held manual surgical instrument intended to be used to cut the malleus (hammer-shaped lateral bone of the group of three that form the sound-transmitting ossicles in the middle ear). It is typically a ring-handled instrument with, distal to a pivot pin, a set of blades: one slides back and forth to operate a set of jaws for cutting, and the other is stationary and may end in a sharpened anvil or a hook. In the anvil design, the sliding blade opens and closes a second sharpened blade against the anvil. In the hook design, the sliding blade closes against the hook. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
JYR	NIPPER, MALLEUS

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: bfd8033e-98bb-4317-be9b-3850d128fcea
Public Version Date: December 11, 2019
Public Version Number: 2
DI Record Publish Date: July 13, 2018