AccessGUDID - DEVICE: ECO Disposable microwave therapeutic antenna (06972405777099)

GUDID

Device Identifier (DI) Information

Brand Name: ECO Disposable microwave therapeutic antenna
Version or Model: ECO-100AL23C
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: ECO Medical Technology (Nanjing) Co., Ltd.

Primary DI Number: 06972405777099
Issuing Agency: GS1
Commercial Distribution End Date: December 02, 2022
Device Count: 1
Labeler D-U-N-S® Number*: 546257098 *Terms of Use

Device Description: Disposable Microwave Therapeutic Antennas is composed of radiator, handle, microwave cable with cooling tubes.

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?
61286	Microwave ablation system probe, non-powered	A non-active, hand-held surgical instrument designed to connect to a microwave ablation system generator to deliver microwaves to a targeted operative site for localized soft-tissue ablation, typically to treat tumours, hydatid cysts and/or menorrhagia. The probe includes a handle and a patient contact region (e.g., antenna, leaflets), and might include a cooling mechanism (via water irrigation). The device is intended to be used in percutaneous, endoscopic [e.g., gastroscopic, laparoscopic], natural orifice or open surgery procedures to ablate tissues (e.g., endometrial ablation). This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
NEY	System, Ablation, Microwave And Accessories

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K201265	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: 9c35fe55-4a31-4837-8a3b-b9b24973dadc
Public Version Date: October 18, 2023
Public Version Number: 3
DI Record Publish Date: November 02, 2022