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Stealth Autoguide

FDA UDI

Class II (US FDA UDI)

by Medtronic Navigation, Inc.

Identity

Trade Name
Stealth Autoguide FDA UDI
Generic Name
Brain biopsy procedure kit FDA UDI
Device Name
REDUCING TUBE 2.4MM 28336 SEEG AUTOGUIDE FDA UDI
Model / Reference
28336 FDA UDI
Description
REDUCING TUBE 2.4MM 28336 SEEG AUTOGUIDE FDA UDI

Identifiers

Primary DI / UDI-DI
00763000536381 FDA UDI
510(k) Number
K191597 FDA UDI
FDA Product Code
HAW FDA UDI
GMDN Term
Brain biopsy procedure kit 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

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Brain biopsy procedure kit

Stealth Autoguide by Medtronic Navigation, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Brain biopsy procedure kit.

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 864e7c63-7d3e-4cd1-a29f-e4da811ae027 35 fields · synced May 30, 2026