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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
Laboratory analyser cuvette IVD, single-use FDA UDI
Device Name
500 mL Wide-Mouth Specimen Containers without Lids FDA UDI
Model / Reference
220-9500-03K FDA UDI
Description
500 mL Wide-Mouth Specimen Containers without Lids FDA UDI

Identifiers

Catalog Number
220-9500-03K FDA UDI
Primary DI / UDI-DI
00810044201017 FDA UDI
FDA Product Code
NNI FDA UDI
GMDN Term
Laboratory analyser cuvette IVD, single-use 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: Laboratory analyser cuvette IVD, single-use

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

Similar devices

Also classified as Laboratory analyser cuvette IVD, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Caplugs, Inc.

Sources (1)

  • FDA UDI 207ad698-b22e-4d57-865c-3978a1bf69b0 35 fields · synced Jun 9, 2026