Capette

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name: Capette FDA UDI
Generic Name: Personal device holder, single-use FDA UDI
Device Name: Small Capette™ with small tube tackles. FDA UDI
Model / Reference: CP-4201 FDA UDI
Description: Small Capette™ with small tube tackles. FDA UDI

Identifiers

Primary DI / UDI-DI: 00709078012990 FDA UDI
FDA Product Code: JAY FDA UDI
GMDN Term: Personal device holder, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5280 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Personal device holder, single-use

Capette by Westmed, Inc. — 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: Westmed, Inc.

Sources (1)

FDA UDI 4ce297d2-6f93-4021-b2f7-9b00afc4c3e5 33 fields · synced Jun 8, 2026