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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
Inoculating tool IVD, analyser/instrument FDA UDI
Device Name
2-SPLIT INOCULUM TRAY FDA UDI
Model / Reference
222-8122-01T FDA UDI
Description
2-SPLIT INOCULUM TRAY FDA UDI

Identifiers

Catalog Number
222-8122-01T FDA UDI
Primary DI / UDI-DI
00810044208078 FDA UDI
FDA Product Code
JTC FDA UDI
GMDN Term
Inoculating tool IVD, analyser/instrument FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2500 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: Inoculating tool IVD, analyser/instrument

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

Similar devices

Also classified as Inoculating tool IVD, analyser/instrument.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Caplugs, Inc.

Sources (1)

  • FDA UDI bb5670a6-5f63-42aa-a8af-9758e2e06f29 35 fields · synced Jun 9, 2026