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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 laboratory container, single-use, sterile FDA UDI
Device Name
TEST TUBE 17X100MM 2-POS CAP FDA UDI
Model / Reference
500 FDA UDI
Description
TEST TUBE 17X100MM 2-POS CAP FDA UDI

Identifiers

Catalog Number
222-2393-080 FDA UDI
Primary DI / UDI-DI
00810044204773 FDA UDI
FDA Product Code
LIB FDA UDI
GMDN Term
General laboratory container, single-use, sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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 laboratory container, single-use, sterile

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

Similar devices

Also classified as General laboratory container, single-use, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Caplugs, Inc.

Sources (1)

  • FDA UDI 8eb4cce6-36b8-4a51-b38d-8160e6811d97 35 fields · synced Jun 9, 2026