← Back to catalogue
Thd Light-Scope Maxi-Recto (led Ins/Ns)
EUDAMEDFDA UDIClass I (EU MDR)
Ref 800099Model THD Not Sterile AnoProctoRectoscopes LED and not LED
by Thd S.p.a.
Identity
- Trade Name
- THD LIGHT-SCOPE MAXI-RECTO (LED INS/NS) EUDAMEDTHD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope FDA UDI
- Generic Name
- Optical anoscope, single-use FDA UDI
- Device Name
- THD Not Sterile AnoProctoRectoscopes LED and not LED EUDAMEDThe Light-Scope LED rectoscope is a disposable medical device deemed for investigation of the anal canal and of the distal region of the sigma. The Light-Scope LED rectoscope combines in a single device a magnifier lens and a powerful, fully integrated, LED light source, in order to have a clear and detailed vision of the inspection field. The Light-Scope LED rectoscope is ready-to-use and it also available with an inflating included. FDA UDI
- Model / Reference
- THD Not Sterile AnoProctoRectoscopes LED and not LED EUDAMED800099 EUDAMEDTHD Light - Scope LED Large Rectoscope with inflation bulb Not Sterile FDA UDI
- Description
- The Light-Scope LED rectoscope is a disposable medical device deemed for investigation of the anal canal and of the distal region of the sigma. The Light-Scope LED rectoscope combines in a single device a magnifier lens and a powerful, fully integrated, LED light source, in order to have a clear and detailed vision of the inspection field. The Light-Scope LED rectoscope is ready-to-use and it also available with an inflating included. FDA UDI
Identifiers
- Catalog Number
- 800099 FDA UDI
- Primary DI / UDI-DI
- 08033737710456 EUDAMEDFDA UDI
- Basic UDI-DI
- 803373771DIANS0002Y3 EUDAMED
- FDA Product Code
- FER FDA UDIGCP FDA UDI
- EMDN Code
- G02060302 RIGID PROCTOSCOPES EUDAMED
- GMDN Term
- Optical anoscope, single-use FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Market of Registration
- Italy EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 240 Millimeter FDA UDIOuter Diameter — 20 Millimeter FDA UDI
Thd Light-Scope Maxi-Recto (led Ins/Ns) by Thd S.p.a. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 803373771DIANS0002Y3 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Thd S.p.a.
- EUDAMED SRN
- IT-MF-000029427
Sources (2)
- EUDAMED b63dd408-c30d-4ca6-883e-290543e678c0 61 fields · synced Jul 30, 2026
- FDA UDI ad1c3e26-b9b5-400e-b2b1-9abb23eff9be 36 fields · synced May 30, 2026