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Additive Cap

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
Additive Cap FDA UDI
Generic Name
Medicine bottle cap FDA UDI
Device Name
Additive Cap (Non-Sterile) for PAB® Bags FDA UDI
Model / Reference
N2140 FDA UDI
Description
Additive Cap (Non-Sterile) for PAB® Bags FDA UDI

Identifiers

Catalog Number
N2140 FDA UDI
Primary DI / UDI-DI
04046964186936 FDA UDI
FDA Product Code
KPE FDA UDI
GMDN Term
Medicine bottle 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medicine bottle cap

Additive Cap by B. Braun Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medicine bottle cap.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 66b81d56-9cfb-4422-a176-cdb6c879b059 35 fields · synced May 31, 2026