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-190N FDA UDI

Identifiers

Catalog Number: 2SC-190N FDA UDI
Primary DI / UDI-DI: 00841823100016 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

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

Sterilization Method

Ethylene Oxide 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 9a10a9e7-4347-460c-bf03-351349936b32 35 fields · synced Jun 9, 2026