AccessGUDID - DEVICE: PENADAPT (20845854061081)

GUDID

Device Identifier (DI) Information

Brand Name: PENADAPT
Version or Model: MEDLPA2010
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: MEDLPA2010
Company Name: Conmed Corporation

Primary DI Number: 20845854061081
Issuing Agency: GS1
Commercial Distribution End Date: November 18, 2021
Device Count: 36
Labeler D-U-N-S® Number*: 071595540 *Terms of Use

Device Description: Electrosurgery Pencil adapter with 3/8 Inch (.952cm) x 4 Foot (121.92cm) connected to 7/8 Inch (2.22cm) x 6 Foot (1.8288m) Hose

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?
46483	Surgical plume evacuation system tube	A long, hollow cylinder which, as part of a surgical plume evacuation system, is intended to be used to capture, conduct, and exhaust the plume of smoke generated during open surgical procedures in which there is tissue ablation (e.g., laser surgery, electrocautery, electrosurgical diathermy device). This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FYD	APPARATUS, EXHAUST, SURGICAL

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: 661448bd-fe38-4729-9f8a-cab698d793b5
Public Version Date: May 03, 2024
Public Version Number: 3
DI Record Publish Date: June 18, 2020