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Thd Maxi-Recto (ns)
EUDAMEDFDA UDIClass I (EU MDR)
Ref 800077Model THD Not Sterile AnoProctoRectoscopes LED and not LED
by Thd S.p.a.
Identity
- Trade Name
- THD MAXI-RECTO (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 EUDAMEDTheTHD rectoscope is a disposable medical device deemed for investigation of the anal canal and of the distal region of the sigma. FDA UDI
- Model / Reference
- THD Not Sterile AnoProctoRectoscopes LED and not LED EUDAMED800077 EUDAMEDRectoscope Large Not Sterile FDA UDI
- Description
- TheTHD rectoscope is a disposable medical device deemed for investigation of the anal canal and of the distal region of the sigma. FDA UDI
Identifiers
- Catalog Number
- 800077 FDA UDI
- Primary DI / UDI-DI
- 08033737710388 EUDAMEDFDA UDI
- Basic UDI-DI
- 803373771DIANS0001XZ EUDAMED
- FDA Product Code
- GCP FDA UDIFER 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
- Outer Diameter — 20 Millimeter FDA UDILength — 240 Millimeter FDA UDI
Thd Maxi-Recto (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 | 803373771DIANS0001XZ | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Thd S.p.a.
- EUDAMED SRN
- IT-MF-000029427
Sources (2)
- EUDAMED 9e1fcef4-515a-4cac-95ec-dfc445ff2405 61 fields · synced Jul 11, 2026
- FDA UDI 237b1710-e816-47f5-a554-1f1b1ca0ad74 36 fields · synced May 29, 2026