AccessGUDID - DEVICE: Tissue-Tek® Glas™ g2 (00615233080646)

GUDID

Device Identifier (DI) Information

Brand Name: Tissue-Tek® Glas™ g2
Version or Model: 6417
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 6417
Company Name: SAKURA FINETEK U.S.A., INC.

Primary DI Number: 00615233080646
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 179135769 *Terms of Use

Device Description: Coverslips 24 x 60 mm; 200 coverslips; 5 holders/case

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:	Yes
Prescription Use (Rx):	No
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?
42833	Microscope slide holder, preparation/staining	A holder used in the laboratory to hold microscope slides in an upright position during the preparation or staining procedures. It is typically made of plastic materials, will sit sturdily upon a flat surface (e.g., a laboratory bench top or on a shelf) and has a series of spaced slots into which the slides are placed. This is a reusable device.	Active	false
15687	Microscope slide coverslip IVD	A thin piece of glass or a plastic sheath placed over a specimen on a microscope slide, to serve as a physical barrier to protect the specimen from mechanical forces and environmental exposure. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KES	COVERSLIPS, MICROSCOPE SLIDE

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: No

Sterilization Method [?]
No Sterilization Methods Found

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: 699ecafd-2670-4167-8601-827bf9dcafe0
Public Version Date: August 20, 2020
Public Version Number: 2
DI Record Publish Date: February 06, 2020