AccessGUDID - DEVICE: Olympus (06939029815088)

GUDID

Device Identifier (DI) Information

Brand Name: Olympus
Version or Model: WA98210B
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Modern Medical Equipment MFG. Ltd.

Primary DI Number: 06939029815088
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 527812392 *Terms of Use

Device Description: Disposable Button Switch Pencil ,Coated Electrode Blade.White color of pencil with 3m color blue Cable ,3 prong plug .Standard hex over mold blade with Teflon Coated .

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):	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?
61869	Open-surgery electrosurgical handpiece/electrode, monopolar, single-use	A rigid device consisting of combined electrosurgical handpiece and monopolar electrode intended to deliver electrosurgical current from a system generator directly to tissues for cutting/coagulation during an open surgical procedure. It is available in a variety of forms (e.g., pen, pistol-shaped forceps, pincer-shaped forceps, scissors) and may also include irrigation, aspiration, lavage and/or surgical plume (smoke) evacuation features to support its primary electrosurgical function. This is a single-use device intended to be used in a sterile condition.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GEI	Electrosurgical, Cutting & Coagulation & Accessories

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: Yes
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Ethylene Oxide

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: f4f1b7d7-09f3-4a9c-a70c-5c58dd4a1a9d
Public Version Date: February 07, 2019
Public Version Number: 3
DI Record Publish Date: October 31, 2017

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Status	Package Type
36939029815089	100	26939029815082	In Commercial Distribution	Shipping Carton
16939029815085	10	06939029815088	In Commercial Distribution	Dispensary Box
26939029815082	50	16939029815085	In Commercial Distribution	Inner Box