← Back to catalogue

Thd M-Procto (tr/Ns)

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 800029Model THD Not Sterile AnoProctoRectoscopes LED and not LED

by Thd S.p.a.

Identity

Trade Name
THD M-PROCTO (TR/NS) EUDAMED
THD 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 EUDAMED
The THD proctoscope is a disposable medical device deemed for examination and treatment of the anal and rectum Available with truncated or beveled tip. FDA UDI
Model / Reference
THD Not Sterile AnoProctoRectoscopes LED and not LED EUDAMED
800029 EUDAMED
Truncated Proctoscope Medium Not Sterile FDA UDI
Description
The THD proctoscope is a disposable medical device deemed for examination and treatment of the anal and rectum Available with truncated or beveled tip. FDA UDI

Identifiers

Catalog Number
800029 FDA UDI
Primary DI / UDI-DI
08033737710081 EUDAMEDFDA UDI
Basic UDI-DI
803373771DIANS0001XZ EUDAMED
FDA Product Code
GCP FDA UDI
FER FDA UDI
EMDN Code
Z12020603 PROCTOSCOPES EUDAMED
GMDN Term
Optical anoscope, single-use FDA UDI

Classification

Device Class
Class I EUDAMED
Class 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 — 22.1 Millimeter FDA UDI
Length — 130 Millimeter FDA UDI

Category: Sphincteroscope

Thd M-Procto (tr/Ns) by Thd S.p.a. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sphincteroscope.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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 dc57d863-45da-4c1b-a3aa-0507eb4da02f 61 fields · synced Jul 18, 2026
  • FDA UDI bbe1d871-5c47-4871-9a97-6a5fc284e385 36 fields · synced May 30, 2026