Infrastructure

Manufacturing systems built for clean, consistent suture production.

From controlled clean room conditions to validated sterilization and protective packaging, GMD Group infrastructure supports product reliability at every production stage.

Process Integrity

Clean room control
Sterilization discipline
Protective packaging

ISO 0

Clean room equivalent standard

HEPA filtration efficiency down to 0.3 micron

Core infrastructure stages

01 Clean Room

Controlled Environment

Clean Room

A controlled clean room environment helps minimize particulate and microbial contamination during production.

GMD uses a clean room facility designed to meet Class 10,000 / ISO Class 7 standards, supported by HEPA filtration and controlled material transfer.

ISO Class 7 environment
HEPA filtered process areas
Air locks and pass boxes

02 Sterilization

Validated Sterility

Sterilization

Sterilization is performed with 100% pure ethylene oxide gas in a controlled process designed for reliable sterility.

The cycle considers moisture-sensitive absorbable sutures to help protect product strength and storage performance.

100% pure ethylene oxide gas
Moisture-aware sterilization cycle
Designed for absorbable sutures

03 Packaging

Product Protection

Packaging

Packaging protects moisture-sensitive sutures from conditions that may affect tensile strength and absorption properties.

Vacuuming and nitrogen flushing support a stronger moisture barrier and help maintain long shelf-life performance.

Moisture-resistant barrier
Vacuum and nitrogen flushing
Long shelf-life support

GMD Group

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