AccessGUDID - DEVICE: THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope (08033737710562)

GUDID

Device Identifier (DI) Information

Brand Name: THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope
Version or Model: THD Light-Scope_Rectoscope Medium with inflation bulb_Sterile
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 800121
Company Name: THD SPA

Primary DI Number: 08033737710562
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 338430324 *Terms of Use

Device Description: 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

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":	Yes
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?
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.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FER	Anoscope And Accessories
GCP	Endoscope, Ac-Powered And Accessories

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: 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
Outer Diameter: 20 Millimeter
Length: 190 Millimeter

Device Record Status

Public Device Record Key: 5fcc330f-5145-4f4a-8f03-1e4c517d6dd2
Public Version Date: October 28, 2024
Public Version Number: 5
DI Record Publish Date: December 23, 2016