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Navigator 3 Wireless Probe, 14 mm Angled

FDA UDI

Class I (US FDA UDI)

by crystal-photonics GmbH

Identity

Trade Name
Navigator 3 Wireless Probe, 14 mm Angled FDA UDI
Generic Name
Hand-held-detector nuclear medicine system FDA UDI
Device Name
gamma probe system, angled wireless probe FDA UDI
Model / Reference
CXS-OP-AP-WP FDA UDI
Description
gamma probe system, angled wireless probe FDA UDI

Identifiers

Catalog Number
200297 FDA UDI
Primary DI / UDI-DI
04260152884507 FDA UDI
FDA Product Code
IZD FDA UDI
GMDN Term
Hand-held-detector nuclear medicine system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1320 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

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Hand-held-detector nuclear medicine system

Navigator 3 Wireless Probe, 14 mm Angled by crystal-photonics GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held-detector nuclear medicine system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1fbe0f0d-0c00-4369-8123-de634cdf3873 34 fields · synced May 30, 2026