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Mectascope

FDA UDI

Class II (US FDA UDI)

by Medacta International

Identity

Trade Name
Mectascope FDA UDI
Generic Name
Rigid endoscope telescope FDA UDI
Device Name
MectaScope - Rotating Sheath,Double stopcock, WL=15cm FDA UDI
Model / Reference
05.17.10.0005 FDA UDI
Description
MectaScope - Rotating Sheath,Double stopcock, WL=15cm FDA UDI

Identifiers

Primary DI / UDI-DI
07630040733526 FDA UDI
510(k) Number
K200067 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Rigid endoscope telescope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Category: Rigid endoscope telescope

Mectascope by Medacta International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscope telescope.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7be86d95-cc22-4210-bd62-6c43e24015a3 34 fields · synced Jun 8, 2026