← Back to catalogue

MD Ophthalmic Dropper Bottles

FDA UDI

Class I (US FDA UDI)

by Medisca Inc.

Identity

Trade Name
MD Ophthalmic Dropper Bottles FDA UDI
Generic Name
Eye dropper bottle FDA UDI
Device Name
MD Ophthalmic Dropper Bottles, 10 mL, Sterile, Ready-to-fill, Clear with White Caps FDA UDI
Model / Reference
5591-03 FDA UDI
Description
MD Ophthalmic Dropper Bottles, 10 mL, Sterile, Ready-to-fill, Clear with White Caps FDA UDI

Identifiers

Catalog Number
5591-03 FDA UDI
Primary DI / UDI-DI
00338779559130 FDA UDI
FDA Product Code
KYX FDA UDI
GMDN Term
Eye dropper bottle FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6430 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Eye dropper bottle

MD Ophthalmic Dropper Bottles by Medisca Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Eye dropper bottle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medisca Inc.

Sources (1)

  • FDA UDI 4a0cfff1-178d-4cd0-956f-d44c42990797 34 fields · synced May 30, 2026