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21ga 600mm Always-On Tip Tracked Stylet, Blunt Tip

FDA UDI

Class II (US FDA UDI)

by Veran Medical Technologies Inc.

Identity

Trade Name
21ga 600mm Always-On Tip Tracked Stylet, Blunt Tip FDA UDI
Generic Name
Electromagnetic surgical navigation device tracking system FDA UDI
Model / Reference
INS-5200 FDA UDI

Identifiers

Catalog Number
INS-5200 FDA UDI
Primary DI / UDI-DI
00815686020422 FDA UDI
510(k) Number
K093146 FDA UDI
FDA Product Code
JAK FDA UDI
GMDN Term
Electromagnetic surgical navigation device tracking system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1750 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

21ga 600mm Always-On Tip Tracked Stylet, Blunt Tip by Veran Medical Technologies Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5300edfc-336f-4dbb-8696-4c347aaf11da 35 fields · synced May 30, 2026