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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
Medical tubing clip/clamp, temporary, non-calibrated, single-use FDA UDI
Device Name
PINNACLE® TPN Bag Tamper Resistant Clamps, 1 L or larger FDA UDI
Model / Reference
2112397 FDA UDI
Description
PINNACLE® TPN Bag Tamper Resistant Clamps, 1 L or larger FDA UDI

Identifiers

Catalog Number
2112397 FDA UDI
Primary DI / UDI-DI
04046964201349 FDA UDI
FDA Product Code
KPE FDA UDI
GMDN Term
Medical tubing clip/clamp, temporary, non-calibrated, single-use 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

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: Medical tubing clip/clamp, temporary, non-calibrated, single-use

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

Similar devices

Also classified as Medical tubing clip/clamp, temporary, non-calibrated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
B. Braun Medical Inc.

Sources (1)

  • FDA UDI 58f43b1e-5755-4f97-b2ea-f42db16edded 35 fields · synced Jun 1, 2026