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TV-3 Camera Control Unit Aurora II, 3, and Four Series

FDA UDI

Class I (US FDA UDI)

by Skytron, LLC

Identity

Trade Name
TV-3 Camera Control Unit Aurora II, 3, and Four Series FDA UDI
Generic Name
Surgical video camera FDA UDI
Device Name
Remote Camera control unit for Precision HD for Aurora II AUR and up. FDA UDI
Model / Reference
B1-710-59 FDA UDI
Description
Remote Camera control unit for Precision HD for Aurora II AUR and up. FDA UDI

Identifiers

Primary DI / UDI-DI
10841736112134 FDA UDI
FDA Product Code
KQM FDA UDI
GMDN Term
Surgical video camera FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4160 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

TV-3 Camera Control Unit Aurora II, 3, and Four Series by Skytron, LLC — Class I — 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

Manufacturer
Skytron, LLC

Sources (1)

  • FDA UDI 2ac16f09-5776-4ff4-84c8-1afb7f2eddc1 35 fields · synced May 30, 2026