Seeg Sst Cannula Adaptor Ø3.2mm

FDA UDI

Class II (US FDA UDI)

by Medtech Llc

Identity

Trade Name: SEEG SST CANNULA ADAPTOR Ø3.2MM FDA UDI
Generic Name: Multi-purpose stereotactic surgery system FDA UDI
Device Name: SEEG Cannula Adaptor Ø3.20 mm instrument Rosa 3.0 instrument Rosa 3.1 stainless steel instrument adaptor to accomodate surgical drill through a 3,20 mm diameter cannula. Not for drilling FDA UDI
Model / Reference: ROSA3-281A FDA UDI
Description: SEEG Cannula Adaptor Ø3.20 mm instrument Rosa 3.0 instrument Rosa 3.1 stainless steel instrument adaptor to accomodate surgical drill through a 3,20 mm diameter cannula. Not for drilling FDA UDI

Identifiers

Catalog Number: ROSAS00091 FDA UDI
Primary DI / UDI-DI: 03760244031631 FDA UDI
FDA Product Code: HAW FDA UDI
GMDN Term: Multi-purpose stereotactic surgery system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.4560 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Neurological stereotactic surgery system Multi-purpose stereotactic surgery system

Seeg Sst Cannula Adaptor Ø3.2mm by Medtech Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Medtech Llc

Sources (1)

FDA UDI 48fb10f4-15f8-42f1-b1e3-315d62d98c18 34 fields · synced May 30, 2026