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Caspar Drill Guide

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
CASPAR DRILL GUIDE FDA UDI
Generic Name
Ophthalmic surgical instrument handle quick lock adaptor FDA UDI
Device Name
CASPAR DRILL GUIDE RIGHT HANDED FDA UDI
Model / Reference
416-340 FDA UDI
Description
CASPAR DRILL GUIDE RIGHT HANDED FDA UDI

Identifiers

Catalog Number
416-340 FDA UDI
Primary DI / UDI-DI
00192896037267 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Ophthalmic surgical instrument handle quick lock adaptor 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ophthalmic surgical instrument handle quick lock adaptor

Caspar Drill Guide by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgical instrument handle quick lock adaptor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 96acd0d3-9a4b-4926-8931-43ca1b495fc0 36 fields · synced May 30, 2026