AccessGUDID - DEVICE: Coblation (00817470002041)

GUDID

Device Identifier (DI) Information

Brand Name: Coblation
Version or Model: KP-CAV-7700-01
Commercial Distribution Status: In Commercial Distribution
Catalog Number: KP-CAV-7700-01
Company Name: Smith & Nephew, Inc.

Primary DI Number: 00817470002041
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 045483575 *Terms of Use

Device Description: CAVITY 11 GAUGE

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?
35703	Universal foot-controlled electrosurgical diathermy system conducting unit, single-use	A sterile electrical conductor comprised of an electrode handpiece with cables and an active electrode, typically non-detachable, intended to provide an electrical connection between the output terminals of an electrosurgical diathermy generator and a patient. The energy emitted from the device is used to cut and coagulate tissue at a surgical site on the patient. The operator regulates the energy with a foot-switch. This is a non-dedicated device intended to be used in multiple clinical specialties. This is a single-use device.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
GEI	ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K063172	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
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: 7b228c72-e8f8-4adf-9dd1-553dbaa5d473
Public Version Date: September 07, 2023
Public Version Number: 5
DI Record Publish Date: August 29, 2015