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Marina Medical

FDA UDI

Class I (US FDA UDI)

by Marina Medical Instruments, Inc.

Identity

Trade Name
Marina Medical FDA UDI
Generic Name
Ophthalmic calliper FDA UDI
Device Name
Castroviejo Caliper Graduated 0-20mm, 8.5cm FDA UDI
Model / Reference
190-546 FDA UDI
Description
Castroviejo Caliper Graduated 0-20mm, 8.5cm FDA UDI

Identifiers

Catalog Number
190-546 FDA UDI
Primary DI / UDI-DI
00840306804700 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Length — 8.5 Centimeter FDA UDI

Category: Ophthalmic calliper

Marina Medical by Marina Medical Instruments, 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 5ea2d2f1-2fe4-4ceb-9238-eac0c10b9831 36 fields · synced May 30, 2026