← Back to catalogue

Tilcare

FDA UDI

Class I (US FDA UDI)

by Tilco Trading Pte. Ltd.

Identity

Trade Name
Tilcare FDA UDI
Generic Name
Oral liquid dose dispenser cabinet FDA UDI
Device Name
Oral Dispenser with Cover 3ml FDA UDI
Model / Reference
ORAL DISPENSER WITH COVER 3ML FDA UDI
Description
Oral Dispenser with Cover 3ml FDA UDI

Identifiers

Primary DI / UDI-DI
05060665920469 FDA UDI
FDA Product Code
KYX FDA UDI
GMDN Term
Oral liquid dose dispenser cabinet 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

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Total Volume — 3 Milliliter FDA UDI

Category: Oral liquid dose dispenser cabinet

Tilcare by Tilco Trading Pte. Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oral liquid dose dispenser cabinet.

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

Sources (1)

  • FDA UDI 45a7427c-945e-4af8-b300-aa38e0e75444 35 fields · synced May 31, 2026