AccessGUDID - DEVICE: EYEPIECE CAP (04953170063749)

GUDID

Device Identifier (DI) Information

Brand Name: EYEPIECE CAP
Version or Model: MB-147
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: OLYMPUS MEDICAL SYSTEMS CORP.

Primary DI Number: 04953170063749
Issuing Agency: GS1
Commercial Distribution End Date: August 12, 2022
Device Count: 1
Labeler D-U-N-S® Number*: 711789789 *Terms of Use

Device Description: No description.

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):	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?
65470	Scope eyepiece attachment	A soft contouring device intended to be attached to the eyepiece of a medical scope (e.g., endoscope, ophthalmoscope, microscope) to provide comfort for, or assist positioning of, the eye during use of the scope; it is not a storage cover. It may be in the form of a covering, brow rest, or eyecup and is typically intended for contact with a healthcare professional while performing a procedure, but some types are intended for contact with the patient while being viewed with an opthalmoscope; it does not include optics. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FDF	Colonoscope And Accessories, Flexible/Rigid
FDS	Gastroscope And Accessories, Flexible/Rigid
FDT	Duodenoscope And Accessories, Flexible/Rigid
ODG	Endoscopic Ultrasound System, Gastroenterology-Urology

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
No Device Sizes

Device Record Status

Public Device Record Key: e146c352-7206-4ab2-a9f4-ebe403544ece
Public Version Date: January 16, 2023
Public Version Number: 3
DI Record Publish Date: December 20, 2021