Two-Piece Slotted Cannula

FDA UDI

Class I (US FDA UDI)

by Ad-Tech Medical Instrument Corp.

Identity

Trade Name: Two-Piece Slotted Cannula FDA UDI
Generic Name: Neurological stereotactic surgery system FDA UDI
Model / Reference: 2SC-240X FDA UDI

Identifiers

Catalog Number: 2SC-240X FDA UDI
Primary DI / UDI-DI: 00841823100047 FDA UDI
FDA Product Code: GEA FDA UDI
GMDN Term: Neurological stereotactic surgery system FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Neurological stereotactic surgery system

Two-Piece Slotted Cannula by Ad-Tech Medical Instrument Corp. — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Ad-Tech Medical Instrument Corp.

Sources (1)

FDA UDI 38b7ae8b-4b5c-4020-81e4-41c204c500de 35 fields · synced Jun 9, 2026