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Starter Kit

FDA UDI

Class II (US FDA UDI)

by Civco Medical Instruments Co., Inc.

Identity

Trade Name
Starter Kit FDA UDI
Generic Name
Electromagnetic surgical navigation device tracking system FDA UDI
Device Name
Reusable non-sterile Volume Navigation Sensor bracket with (9 x 91.5cm) CIV-Flex™ covers (5) for use with GE Healthcare C3-10-D transducers FDA UDI
Model / Reference
H40482LF FDA UDI
Description
Reusable non-sterile Volume Navigation Sensor bracket with (9 x 91.5cm) CIV-Flex™ covers (5) for use with GE Healthcare C3-10-D transducers FDA UDI

Identifiers

Catalog Number
H40482LF FDA UDI
Primary DI / UDI-DI
00841436108904 FDA UDI
510(k) Number
K092619 FDA UDI
FDA Product Code
IYO FDA UDI
GMDN Term
Electromagnetic surgical navigation device tracking system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1560 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

Yes

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

Dimensions & Sizes

Size
Width — 1.92 Inch FDA UDI
Length — 1.88 Inch FDA UDI

Category: Electromagnetic surgical navigation device tracking system

Starter Kit by Civco Medical Instruments Co., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electromagnetic surgical navigation device tracking system.

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 216225db-d94c-4dbc-a90a-60dd76249f88 38 fields · synced Jun 8, 2026