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Caplugs/Evergreen

FDA UDI

Class I (US FDA UDI)

by Caplugs, Inc.

Identity

Trade Name
Caplugs/Evergreen FDA UDI
Generic Name
General specimen container IVD, no additive/medium FDA UDI
Device Name
MOISTURE CHAMBER NATURAL FDA UDI
Model / Reference
240-9000-010 FDA UDI
Description
MOISTURE CHAMBER NATURAL FDA UDI

Identifiers

Catalog Number
240-9000-010 FDA UDI
Primary DI / UDI-DI
00810044207972 FDA UDI
FDA Product Code
FMH FDA UDI
GMDN Term
General specimen container IVD, no additive/medium FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General specimen container IVD, no additive/medium

Caplugs/Evergreen by Caplugs, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General specimen container IVD, no additive/medium.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Caplugs, Inc.

Sources (1)

  • FDA UDI e13e65a1-d6d5-4a1e-b493-d9eb5f0a8914 35 fields · synced Jun 9, 2026