DEVICE: THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope (08033737710579)
Device Identifier (DI) Information
THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope
THD Light-Scope_Rectoscope Large with inflation bulb_Sterile
In Commercial Distribution
800120
THD SPA
THD Light-Scope_Rectoscope Large with inflation bulb_Sterile
In Commercial Distribution
800120
THD SPA
The THD Light-Scope rectoscope is a disposable medical device deemed for investigation of the anal canal and of the distal region of the sigma. The THD Light-Scope rectoscope combines a magnifier lens in the back cap. The handle has a lodgement for a THD Fiber Optic Cable tip for using the rectoscope with a THD light source. The THD Light-Scope rectoscope is ready-to-use and can also be available with an inflation bulb included.
Device Characteristics
Labeling does not contain MRI Safety Information | |
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GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
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44914 | Optical anoscope, single-use |
An endoscope with a rigid inserted portion intended for the visual examination and treatment of the anus and rectum. It is inserted into the body through the anus during anoscopy. The inserted portion is short in length, though longer than a sphincteroscope, and large in diameter, and an obturator is typically inserted into its lumen to assist the insertion. The anatomical images are illuminated by a built-in or external light source and can be viewed by the user through relayed lens optics or direct vision. This device is typically used to examine/diagnose patients suffering pain in the rectum/anus, haemorrhoids, or anal fissures. This is a single-use device.
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FDA Product Code
[?]Product Code | Product Code Name |
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FER | Anoscope And Accessories |
GCP | Endoscope, Ac-Powered And Accessories |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
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No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
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Outer Diameter: 20 Millimeter |
Length: 240 Millimeter |
Device Record Status
659a448e-a969-48cf-9bba-e562baeda9a5
October 28, 2024
5
December 23, 2016
October 28, 2024
5
December 23, 2016
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
18033737710576 | 10 | 08033737710579 | In Commercial Distribution |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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No Secondary DIs found |
Unit of Use DI
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Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+390522634311
Regulatory@thdlab.com
Regulatory@thdlab.com