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Oph. Caliper

FDA UDI

Class I (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name
Oph. Caliper FDA UDI
Generic Name
Ophthalmic calliper FDA UDI
Device Name
Flexible S/S Ruler 6"x1/2" FDA UDI
Model / Reference
08-12105 FDA UDI
Description
Flexible S/S Ruler 6"x1/2" FDA UDI

Identifiers

Catalog Number
08-12105 FDA UDI
Primary DI / UDI-DI
00841668119822 FDA UDI
FDA Product Code
FTY FDA UDI
GMDN Term
Ophthalmic calliper FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Width — 0.5 Inch FDA UDI
Length — 6 Inch FDA UDI

Category: Ophthalmic calliper

Oph. Caliper by Katena Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic calliper.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5cad4802-ce0b-45f5-be2a-05eb33ed8ee6 36 fields · synced Jun 12, 2026