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ASTM F1140 Burst & Creep Test | Medical Packaging

STM F1140 evaluates seal strength in flexible medical packaging using burst and creep pressurization to support ISO 11607 validation.

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ASTM F1140 defines the methods used to evaluate the strength and integrity of flexible medical packaging by applying internal pressurization until a seal or material failure occurs. Burst and creep tests help determine the weakest area of the packaging and what pressure is needed to expose the weakest area.  The weakest area could be within the seal or surrounding material.

What ASTM F1140 Measures

ASTM F1140 evaluates:

  • Seal strength
  • Material resistance to internal pressure
  • Weak points in flexible packaging
  • Early failures caused by sealing parameters or material defects


Q: What is the purpose of F1140?
To measure how much pressure a package can tolerate before failing and locating where the failure occurred.

Test Methods

Burst Test

The package is inflated until it ruptures. This identifies:

  • Seal uniformity issues
  • Weak seals
  • Material weak points
  • Variability in sealing processes

 

Creep Test

The package is inflated to a set pressure and held for a specified time. This identifies:

  • Slow seal failures
  • Stress-induced weaknesses
  • Material creep behavior
  • Seal durability under constant load

How ASTM F1140 Testing Works

  1. Condition samples per ASTM D4332 or equivalent.
  2. Attach the flexible package to the burst/creep equipment so that it remains unrestrained.
  3. Apply internal pressure at a controlled rate.
  4. Record pressure at failure and location of the failure (burst) or time-to-failure (creep).
  5. Document results for statistical analysis and validation reporting.

Packaging Types Commonly Tested

ASTM F1140 applies to:

  • Tyvek pouches
  • Flexible sterile barrier systems
  • Form-fill-seal pouches
  • Laminated structures

POSITION 1

smp_01

ASTM F1140 Test Method Positions

Description: The package is inserted into the test clamp and remains unsupported and untouched during inflation. This allows the material and seals to respond naturally to internal pressure.

Note 1: This position evaluates seal and material strength without external influence.

POSITION 2

Description: The package is clamped and held firmly enough to keep it horizontal, sealed, and straight during inflation without applying undue pressure to the seal. This technique reduces curling of the pouch, which can affect test results.

Note 2: Because operator handling influences repeatability, this position requires training and consistent technique.

POSITION 3

Description: The package is inserted into the test clamp and left untouched during testing, but supported underneath during inflation.

Note 3: Support helps maintain package geometry and can improve consistency across samples.

smp_03

In the Burst Test, air is introduced into the package at a predetermined pressure and flow rate. The porosity (or lack thereof) of the package material determines the inflation rate for the burst test. Because air escapes through the walls of a porous package during inflation, the flow rate must be increased to compensate for the lost air through the walls and create the back pressure in the porous package. This pressure creates the force needed to rupture the seal.

In the Creep Test, a whole package is inflated to a constant pressure, which is then held for a specified time, resulting in a pass / fail result. The Creep Test provides a test for slow shear of the adhesive bond similar to a dead weight hanging on the seal.

ASTM F1140 vs ASTM F88

MethodMeasuresBest For
ASTM F1140Seal strength under internal pressureConfirming real-world pressure tolerance
ASTM F88Mechanical peel forceEvaluating seal uniformity and sealing process performance

ASTM F1140 FAQ

What does ASTM F1140 measure?
Internal pressurization resistance of flexible sterile packaging.
What is the difference between burst and creep?
Burst measures maximum strength; creep measures strength over time.
Is the test destructive?
Yes, the package is inflated until it fails.
Does ASTM F1140 support ISO 11607 validation?
Yes. It is accepted for seal strength and sterile barrier verification.
What packaging types are compatible?
Any flexible sterile barrier system that can be internally pressurized.

Need testing or validation support?

LSO provides comprehensive package testing and validation services under ISO 11607, ASTM, and ISTA standards.