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30ml KwikVial Oral Liquid Container

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 30030Model KwikVial Container

by MedSafety Solutions

Identity

Trade Name
30ml KwikVial Oral Liquid Container EUDAMED
KwikVial Container FDA UDI
Generic Name
Medicine cup, single-use FDA UDI
Device Name
KwikVial Oral Liquid Container EUDAMED
Oral liquid dose dispenser FDA UDI
Model / Reference
KwikVial Container EUDAMED
30030 EUDAMEDFDA UDI
Description
Oral liquid dose dispenser FDA UDI

Identifiers

Catalog Number
30030 FDA UDI
Primary DI / UDI-DI
00853832007002 EUDAMEDFDA UDI
Basic UDI-DI
0085383200710007W EUDAMED
FDA Product Code
KYX FDA UDI
EMDN Code
V0499 CLINICAL USE CONTAINERS (NON-IVD) - OTHER EUDAMED
GMDN Term
Medicine cup, single-use FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
880.6430 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Total Volume — 30 Milliliter FDA UDI

Category: Instrument transport trolley system

30ml KwikVial Oral Liquid Container by MedSafety Solutions — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument transport trolley system.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
MedSafety Solutions
EUDAMED SRN
US-MF-000008537
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 83fbd9a0-0145-4aee-8182-41c3ef2a7f9f 61 fields · synced Jun 19, 2026
  • FDA UDI f26ccba5-4389-4277-9f87-c49c8bf024f8 36 fields · synced May 30, 2026