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Pinnacle®

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
PINNACLE® FDA UDI
Generic Name
Compounding transfer set FDA UDI
Device Name
PINNACLE® 9-Lead Vented Transfer Set FDA UDI
Model / Reference
2112342 FDA UDI
Description
PINNACLE® 9-Lead Vented Transfer Set FDA UDI

Identifiers

Catalog Number
2112342 FDA UDI
Primary DI / UDI-DI
04046964200311 FDA UDI
FDA Product Code
LHI FDA UDI
GMDN Term
Compounding transfer set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Category: Compounding transfer set

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

Similar devices

Also classified as Compounding transfer set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3ff9364b-fa59-4932-b828-db6d3add4a21 35 fields · synced May 30, 2026