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WatchTower

FDA UDI

Class II (US FDA UDI)

by Intai Technology Corporation

Identity

Trade Name
WatchTower FDA UDI
Generic Name
Orthopaedic stereotactic surgery system FDA UDI
Device Name
Universal DRF C FDA UDI
Model / Reference
INS-NAVHDL-C FDA UDI
Description
Universal DRF C FDA UDI

Identifiers

Primary DI / UDI-DI
04719883200310 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
Orthopaedic stereotactic surgery system 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic stereotactic surgery system

WatchTower by Intai Technology Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic stereotactic surgery system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Intai Technology Corporation

Sources (1)

  • FDA UDI 218b9f2a-20cb-45a2-a054-aedb686506b5 34 fields · synced May 30, 2026