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WatchTower

FDA UDI

Class I (US FDA UDI)

by Intai Technology Corporation

Identity

Trade Name
WatchTower FDA UDI
Generic Name
Orthopaedic stereotactic surgery system FDA UDI
Device Name
XL Fixation Pin FDA UDI
Model / Reference
INS-FIXPIN-001 FDA UDI
Description
XL Fixation Pin FDA UDI

Identifiers

Primary DI / UDI-DI
04719883200402 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic stereotactic surgery system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

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 I — 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 df0e9a65-4644-4004-b8b5-f01a389e5f02 34 fields · synced May 30, 2026