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Sigma Virocult

EUDAMEDFDA UDI

Class I (EU MDR)

Ref MW951SENT

by Medical Wire & Equipment Co Bath (Ltd)

Identity

Trade Name
Sigma Virocult FDA UDI
Generic Name
Urogenital specimen collection kit IVD, clinical FDA UDI
Device Name
Sigma Virocult EUDAMED
Mini Sigma Virocult, Screw Vial, 1ml Virocult, Mini Foam FDA UDI
Model / Reference
MW951SENT EUDAMED
N/a FDA UDI
Description
Mini Sigma Virocult, Screw Vial, 1ml Virocult, Mini Foam FDA UDI

Identifiers

Catalog Number
MW951SENT FDA UDI
Primary DI / UDI-DI
05060259070563 EUDAMEDFDA UDI
Basic UDI-DI
B-05060259070563 EUDAMED
510(k) Number
K082472 FDA UDI
FDA Product Code
LIO FDA UDI
EMDN Code
A1102 SAMPLE COLLECTION SWABS WITH TRANSPORT MEDIUM EUDAMED
GMDN Term
Urogenital specimen collection kit IVD, clinical FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
866.2900 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General-purpose absorbent tip applicator/swab, single-use

Sigma Virocult by Medical Wire & Equipment Co Bath (Ltd) — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose absorbent tip applicator/swab, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
GB-MF-000006736
Authorised Representative
Advena Limited MT-AR-000000234

Sources (2)

  • EUDAMED 3292f956-31a2-41e5-ab60-029b9a2b5bb4 61 fields · synced Jun 18, 2026
  • FDA UDI fad568ec-8382-4e23-8ae0-4bea860f08f9 36 fields · synced May 30, 2026