AccessGUDID - DEVICE: BD™ FocalPoint™ Slide Profiler Refurbished (00382904914905)

GUDID

Device Identifier (DI) Information

Brand Name: BD™ FocalPoint™ Slide Profiler Refurbished
Version or Model: 491490
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 491490
Company Name: BECTON, DICKINSON AND COMPANY

Primary DI Number: 00382904914905
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 122561087 *Terms of Use

Device Description: Focal Point Digital Refurb 2

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?
15132	Cell morphology analyser IVD, manual	An electrically-powered manual laboratory instrument intended to be used for the qualitative microscopic examination of blood or other clinical specimens in order to view, count, record and evaluate the morphological characteristics of cells and other biological components. The device typically includes a microscope, camera, monitor and software package.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MNM	READER, CERVICAL CYTOLOGY SLIDE, AUTOMATED

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
Special Storage Condition, Specify: Room Temperature

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: bdeb2c3c-c896-4017-a223-ba4d7db97e06
Public Version Date: October 13, 2023
Public Version Number: 2
DI Record Publish Date: September 08, 2023