AccessGUDID - DEVICE: C1q / FITC control slides (B502BSB3001CS0)

GUDID

Device Identifier (DI) Information

Brand Name: C1q / FITC control slides
Version or Model: control slides, 5
Commercial Distribution Status: In Commercial Distribution
Catalog Number: BSB 3001-CS
Company Name: BIO SB, INC.

Primary DI Number: B502BSB3001CS0
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 102855447 *Terms of Use

Device Description: C1q / FITC Control

Device Characteristics

What MRI safety information does the labeling contain?	MR Safe
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):	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?
31461	Complement component C1q IVD, control	A material which is used to verify the performance of an assay intended to be used for the quantitative measurement of complement cascade component C1q in a clinical specimen.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LJG	Quality Control Slides

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: 61126966-841b-4cae-a2a1-59b8584748fb
Public Version Date: October 08, 2020
Public Version Number: 1
DI Record Publish Date: September 30, 2020