Sigma Transwab

FDA UDI

Class I (US FDA UDI)

by Medical Wire & Equipment Company (Bath), Ltd.

Identity

Trade Name: Sigma Transwab FDA UDI
Generic Name: General specimen collection kit IVD, clinical FDA UDI
Device Name: Sigma Transwab (fecal), Screw Vial, Green cap 2ml Cary Blair, Plastic Foam FDA UDI
Model / Reference: Sigma Transwab FDA UDI
Description: Sigma Transwab (fecal), Screw Vial, Green cap 2ml Cary Blair, Plastic Foam FDA UDI

Identifiers

Catalog Number: MW168S FDA UDI
Primary DI / UDI-DI: 05060259072727 FDA UDI
FDA Product Code: LIO FDA UDI
GMDN Term: General specimen collection kit IVD, clinical FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 866.2900 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Radiation Sterilization FDA UDI

Category: General specimen collection kit IVD, clinical

Sigma Transwab by Medical Wire & Equipment Company (Bath), Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Medical Wire & Equipment Company (Bath), Ltd.

Sources (1)

FDA UDI c8706239-1181-406b-af75-3f2f00180819 34 fields · synced May 31, 2026