KB Medical Group
Manufacturer and global distributor of single-use medical devices and safety-engineered consumables. Product portfolio includes specimen collection devices, safety needles and holders, syringes (including ISO 80369-3/ENFit-compatible enteral products), infusion sets, and oncology infusion components. Operates large-scale sterile production facilities, holds multiple regulatory certifications, and distributes products through established international channels.
Industries
Nr. of Employees
large (251-1000)
Products
Safety blood collection sets
Single-use blood collection sets and multi-sample needles with integrated safety mechanisms and sterile packaging for venous sampling.
Safety needles and needle holders
Sterile safety needles and luer-lock needle holders in multiple gauges and packaging formats designed to reduce sharps injuries.
ENFit-compatible enteral syringes and adaptors
Enteral syringes, caps, and transition adaptors designed to meet ISO 80369-3 specifications for enteral feeding safety and to reduce misconnections.
Reusable ENFit-compliant enteral syringe (O-ring plunger)
Enteral syringe designed with a durable O-ring plunger to support multiple reuse cycles when cleaned and maintained per instructions; intended to balance safety, sustainability, and cost-effectiveness.
Infusion therapy components
Infusion sets, IV cannulas, extension tubing with needle-free injection ports, IV burettes, stopcocks, and scalp vein sets for infusion and IV therapy.
Oncology infusion components
Infusion components intended to reduce healthcare worker and patient exposure to cytotoxic agents during chemotherapy administration.
Safety blood collection sets
Single-use blood collection sets and multi-sample needles with integrated safety mechanisms and sterile packaging for venous sampling.
Safety needles and needle holders
Sterile safety needles and luer-lock needle holders in multiple gauges and packaging formats designed to reduce sharps injuries.
ENFit-compatible enteral syringes and adaptors
Enteral syringes, caps, and transition adaptors designed to meet ISO 80369-3 specifications for enteral feeding safety and to reduce misconnections.
Reusable ENFit-compliant enteral syringe (O-ring plunger)
Enteral syringe designed with a durable O-ring plunger to support multiple reuse cycles when cleaned and maintained per instructions; intended to balance safety, sustainability, and cost-effectiveness.
Infusion therapy components
Infusion sets, IV cannulas, extension tubing with needle-free injection ports, IV burettes, stopcocks, and scalp vein sets for infusion and IV therapy.
Oncology infusion components
Infusion components intended to reduce healthcare worker and patient exposure to cytotoxic agents during chemotherapy administration.
Expertise Areas
- Enteral device development and ISO 80369-3 (ENFit) implementation
- Sterile manufacturing and EO sterilization
- Safety-engineered syringes, needles, and blood collection systems
- Infusion set and IV component manufacturing
Key Technologies
- ISO 80369-3 enteral connector standards
- Reusable O-ring syringe plunger design
- Ethylene oxide (EO) sterilization
- Blister and sterile packaging processes
News & Updates
Major Milestone: Manufacturing Facility Successfully Completes FDA Inspection with Zero Observations
Announcement that a key manufacturing facility completed an on-site FDA inspection with zero observations and zero deficiencies (on-site inspection concluded Aug 21, 2026).
Overview of a reusable ENFit-compliant enteral syringe using a durable O-ring plunger, emphasizing reuse cycles, cost-effectiveness, and suitability for home and institutional care.
Announcement of regional regulatory certification for enteral silicone stomach tubes and enteral syringes to support ISO 80369-3 adoption in a national market.
Report on supplying customized enteral connector variants and bulk-pack syringes to OEMs and regional markets.
Update confirming in-kind donation and processing of enteral feeding products, including a multi-thousand-unit syringe donation to nonprofit distribution partners.
Notice of transition of blood collection tubes to IVDR and related market positioning in Europe.
Major Milestone: Manufacturing Facility Successfully Completes FDA Inspection with Zero Observations
Announcement that a key manufacturing facility completed an on-site FDA inspection with zero observations and zero deficiencies (on-site inspection concluded Aug 21, 2026).
Overview of a reusable ENFit-compliant enteral syringe using a durable O-ring plunger, emphasizing reuse cycles, cost-effectiveness, and suitability for home and institutional care.
Announcement of regional regulatory certification for enteral silicone stomach tubes and enteral syringes to support ISO 80369-3 adoption in a national market.
Report on supplying customized enteral connector variants and bulk-pack syringes to OEMs and regional markets.
Update confirming in-kind donation and processing of enteral feeding products, including a multi-thousand-unit syringe donation to nonprofit distribution partners.
Notice of transition of blood collection tubes to IVDR and related market positioning in Europe.