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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
Specimen container mailer, non-insulated FDA UDI
Device Name
SLIDE JAR ETHYL ALCOHOL FILL FDA UDI
Model / Reference
308-5500-E8K FDA UDI
Description
SLIDE JAR ETHYL ALCOHOL FILL FDA UDI

Identifiers

Catalog Number
308-5500-E8K FDA UDI
Primary DI / UDI-DI
00810044203509 FDA UDI
FDA Product Code
KDT FDA UDI
GMDN Term
Specimen container mailer, non-insulated 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: Specimen container mailer, non-insulated

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

Similar devices

Also classified as Specimen container mailer, non-insulated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Caplugs, Inc.

Sources (1)

  • FDA UDI 22c1734e-60b3-4120-8bcf-9d99a686d12c 35 fields · synced Jun 9, 2026