GreenEgg

DEVICE DESCRIPTION The GreenEgg™ is a sterile, single-use hand held, non-powered pelvic manipulator used for surgical manipulation and transillumination of the rectum and/or vagina. The…

Registry build 21.09.26

DEVICE DESCRIPTION The GreenEgg™ is a sterile, single-use hand held, non-powered pelvic manipulator used for surgical manipulation and transillumination of the rectum and/or vagina. The 30mm diameter polymer tip fluoresces when viewed under a near infrared system PACKAGING CONTENTS A single GreenEgg™ device is CSR wrapped and placed inside a Tyvek header bag in sterile fashion. INDICATIONS FOR USE The EndoGlow GreenEgg™ manipulator is indicated to provide manipulation of the vaginal or rectum during minimally invasive surgical procedures. When viewed with the NIR camera system of a laparoscope or surgical robot, the GreenEgg™ will fluoresce providing transillumination DIRECTIONS FOR USE Confirm exp date. Remove bag from box, open the bag using sterile technique. Transfer the contents of the bag (CSR blue wrapped GreenEgg™ manipulator) to sterile field Once introduced to the field, the CSR wrap can be removed from the device and discarded. The GreenEgg™manipulator is ready for use Insert the GreenEgg™ manipulator into the vagina or rectum and proceed with surgical procedure CONTRAINDICATIONS The GreenEgg™ is a nonpowered, handheld manipulator, do not use it outside of standard surgical protocol or techniques WARNINGS Contents supplied sterile. Do not use if sterile barrier is damaged Do not use the GreenEgg™ if the device has been opened or damaged CAUTION U.S. Federal law restricts this device to sale by or on the order of a physician STORAGE Store at room temp, avoid extreme temps DISPOSAL Dispose of in accordance with all applicable Federal, State, and local Medical/ Hazardous waste practices REUSE PRECAUTION STATEMENT For single use only: Do not reuse, re-process or re-sterilize. Do not reuse, reprocess, or re-sterilize. Attempting to re-sterilize and reuse the product may diminish its intended performance in transilluminating tissue, reducing its effectiveness. To ensure optimal results and patient safety, a new product must be used for each procedure.

1manufacturer
1catalogue number

Who Else Makes It

Registered in Shanghai.

Chinese manufacturers registered for FDA product code EXX
Manufacturer City Province Registered as Device types
Shanghai Medical Instruments (Group) Ltd. Corp. Shanghai Shanghai Contract manufacturer 235

Record

Regulatory record for GreenEgg
Listed by Endoglow, LLC
FDA product code EXX
Device type Probe, Rectal, Non-Powered
Device class Class 1
Regulation 21 CFR 876.4730
Premarket notification Exempt
Record published 2023-07-07

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Special storage condition: Keep out of sunlight
Packaging Shipper of 4
Sizes Length 12.5 in; outer diameter 30 mm

Catalogue Numbers

Catalogue numbers for GreenEgg
Catalogue number Size Status
EP1000-30 Length 12.5 in In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Marina Medical Marina Medical Instruments, Inc. 12
Medicon Medicon eG. Chirurgiemechaniker-Genossenschaft 9
Novo Surgical Inc. Novo Surgical, Inc. 8
Integra® Jarit® Integra LifeSciences Production Corporation 6
Novo Surgical Novo Surgical, Inc. 6
Aesculap Aesculap AG 6
Integra® Miltex® Integra LifeSciences Production Corporation 5
V. Mueller Steris Corporation 4
Millennium Avalign Technologies, Inc. 2
Gimmi Gimmi Gmbh 2
BR Surgical, LLC BR Surgical LLC 1
Ambler Surgical Ambler Surgical, LLC 1

Showing 12 of 14. All products under Probe, Rectal, Non-Powered

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer