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Dropper Bottle System

FDA UDI

Class I (US FDA UDI)

by Mps Pharma & Medical, Inc.

Identity

Trade Name
DROPPER BOTTLE SYSTEM FDA UDI
Generic Name
Eye dropper bottle FDA UDI
Device Name
TE 15ML BS DROPPER BOTTLE, WHITE FDA UDI
Model / Reference
TE15-415-125-BOT-15BRW FDA UDI
Description
TE 15ML BS DROPPER BOTTLE, WHITE FDA UDI

Identifiers

Primary DI / UDI-DI
00810080611825 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Eye dropper bottle

Dropper Bottle System by Mps Pharma & Medical, 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

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Manufacturer

Manufacturer
Mps Pharma & Medical, Inc.

Sources (1)

  • FDA UDI 3e15d83f-d992-471b-ab6d-e8496579a285 33 fields · synced Jun 7, 2026