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Additive Port Cap

FDA UDI

Class II (US FDA UDI)

by International Medical Industries Inc.

Identity

Trade Name
Additive Port Cap FDA UDI
Generic Name
Luer-formatted protective cap FDA UDI
Device Name
Tamper Evident Additive Port Cap for IV Bags - B. Braun PAB/E3, Non-Sterile FDA UDI
Model / Reference
21-01 FDA UDI
Description
Tamper Evident Additive Port Cap for IV Bags - B. Braun PAB/E3, Non-Sterile FDA UDI

Identifiers

Catalog Number
21-01 FDA UDI
Primary DI / UDI-DI
B21221011 FDA UDI
FDA Product Code
KPE FDA UDI
GMDN Term
Luer-formatted protective cap FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5025 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Luer-formatted protective cap

Additive Port Cap by International Medical Industries Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luer-formatted protective cap.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f2e8dac7-769c-45af-b232-26de11dc67dd 34 fields · synced Jun 8, 2026