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Pharmaceutical Pipe Supports — Validated for cGMP

Pipe clamps for WFI, purified water and API process lines. Full material traceability + 3.1 certs.

Pharma piping operates under FDA validation and cGMP scrutiny. Every component needs traceable material certificates, electropolished surfaces and validated cleanability. NIBRO supplies pharmaceutical clamps with full 3.1 material traceability and electropolished finishes down to Ra 0.4 µm.

Why NIBRO
Factory direct since 2006
EU stainless · EN 10204 3.1 traceable
DIN 3567 + DIN 3570 compliant
ISO 9001:2015 certified production
Worldwide shipping in 22 countries
Section 01

Pharma-specific clamp specification

• Material: AISI 316L, dual certified per EN 10204 3.1, heat number traceable to mill.

• Finish: Electropolished, Ra ≤ 0.4 µm on wetted surfaces (Ra ≤ 0.8 µm available standard).

• Hardware: A4-80 cap screws, captive nylock nuts (cleanroom compatible).

• Liner: USP Class VI EPDM or PTFE, available with batch certificate of compliance.

• Documentation: Material cert + dimensional cert + statement of conformity per batch.

FAQ

Frequently asked

We do not test clamps with riboflavin (clamps are not wetted process components in a typical pharma line). For wetted clamps (e.g. integrated saddle drains) we can arrange third-party riboflavin testing on request.

Ready to spec your supports?

Talk to our engineering team. Factory direct from Oisterwijk, Netherlands.

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