AccessGUDID - DEVICE: LAZIC (04250603740339)

GUDID

Device Identifier (DI) Information

Brand Name: LAZIC
Version or Model: 70.039.03 B
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 70.039.03 B
Company Name: Peter Lazic GmbH

Primary DI Number: 04250603740339
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 327681359 *Terms of Use

Device Description: L-LINE CLASSIC MICRO SCISSORS BAYONET UPWARDS CURVED, 220 MM / 8 3/4" WORING END YASARGIL, BLACK COATED

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?
13496	Neurosurgical scissors	A hand-held manual surgical instrument designed to cut tissue (e.g., dura mater, neural soft-tissue) during neurosurgery. It comprises two hinged blades of micro design that cut with a shearing action (i.e., the blades cut as the sharpened edges pass one another as they are closed). It is typically made of metal and is available in various designs. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LRW	Scissors, General, Surgical

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: f9969408-8954-48ce-8441-99437d71c4b7
Public Version Date: May 31, 2021
Public Version Number: 1
DI Record Publish Date: May 21, 2021