AccessGUDID - DEVICE: Segri-Med Single Deposit Container (SDC) (00896317001805)

GUDID

Device Identifier (DI) Information

Brand Name: Segri-Med Single Deposit Container (SDC)
Version or Model: 6017-1
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 6017-1
Company Name: SNYDER INDUSTRIES, INC.

Primary DI Number: 00896317001805
Issuing Agency: GS1
Commercial Distribution End Date: May 01, 2017
Device Count: 1
Labeler D-U-N-S® Number*: 790327076 *Terms of Use

Device Description: SDC is a versatile, "Point of Use" reusable medical waste container. Its 10 and 17 gallon capacity for needles, lab waste, IV bags, and tubing keeps waste collection costs at a minimum.

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):	No
Over the Counter (OTC):	Yes
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?
35429	Sharps container	A hard-walled container designed for the safe deposit and collection of biologically or chemically contaminated used sharps; this includes needles, lancets, scalpel blades, cannulae, or other devices that present a hazard to a healthcare worker or patient if they were to inadvertently have bodily contact with the device and cause themselves an injury. This container is typically designed to be puncture resistant, leak-proof, and closable (usually having a lid that cannot be reopened once closed) and is identified with the universal biohazard symbol on its labelling. It is disposed of when filled to the recommended level, typically by incineration.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FMI	Needle, Hypodermic, Single Lumen

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No 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
Length: 18 Inch
Height: 25 Inch
Width: 13 Inch

Device Record Status

Public Device Record Key: cbb4b9ab-8615-404e-b4e1-e551bdc4a6c1
Public Version Date: August 18, 2023
Public Version Number: 4
DI Record Publish Date: September 27, 2016