← Back to catalogue

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
95 PIN INOCULATOR ASSEMBLY FDA UDI
Model / Reference
222-8600-01A FDA UDI
Description
95 PIN INOCULATOR ASSEMBLY FDA UDI

Identifiers

Catalog Number
222-8600-01A FDA UDI
Primary DI / UDI-DI
00810044208047 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Caplugs, Inc.

Sources (1)

  • FDA UDI a55c28f9-9225-46e2-93ee-d760d06daed7 35 fields · synced Jun 9, 2026