AccessGUDID - DEVICE: V. Mueller (10885403073342)

GUDID

Device Identifier (DI) Information

Brand Name: V. Mueller
Version or Model: NL3760
Commercial Distribution Status: In Commercial Distribution
Catalog Number: NL3760
Company Name: STERIS CORPORATION

Primary DI Number: 10885403073342
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 021599373 *Terms of Use

Device Description: V. Mueller JANNETTA ANGULAR KNIFE SMALL, 2MM DIAMETER OVERALL LENGTH 7-1/2 inches 19.1CM

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?
35135	Dura mater knife	A hand-held manual surgical instrument designed to cut or incise the dura mater without damaging the underlying structures during a surgical intervention. It is typically a one-piece instrument with a sharp, single-edged, cutting blade terminating in a hook shape at the distal end (the internal radius of the hook has the cutting edge) which is normally very small; it has a long slender shaft with a handle at the proximal end. It is normally made of high-grade stainless steel. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HAO	INSTRUMENT, SURGICAL, NON-POWERED

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: 7ec2ed01-4c4a-47ab-8d3f-b725709c7433
Public Version Date: August 22, 2024
Public Version Number: 4
DI Record Publish Date: August 30, 2018