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House Ear Caliper

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
HOUSE EAR CALIPER FDA UDI
Generic Name
General-purpose calliper, metallic FDA UDI
Device Name
HOUSE EAR CALIPER WITH ROD MARK FDA UDI
Model / Reference
1463-140 FDA UDI
Description
HOUSE EAR CALIPER WITH ROD MARK FDA UDI

Identifiers

Catalog Number
1463-140 FDA UDI
Primary DI / UDI-DI
00192896059009 FDA UDI
FDA Product Code
KTZ FDA UDI
GMDN Term
General-purpose calliper, metallic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4150 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

Dimensions & Sizes

Size
Length — 6.25 Inch FDA UDI

Category: General-purpose calliper, metallic

House Ear Caliper by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose calliper, metallic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 631ecf17-67e2-496f-9086-80d9a398f7d0 36 fields · synced May 30, 2026