OEM & PRIVATE LABEL
We manage complete OEM and private-label surgical instrument programs — from specification and artwork approval through to CE and FDA-compliant branded delivery — for medical device brands and distributors worldwide.
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OEM PROGRAM OVERVIEW
Bio Tech Globals manages complete OEM and white-label surgical instrument programs for medical device brands, wholesale distributors and hospital procurement teams building their own branded instrument lines. Every program spans initial specification and brand asset submission, through instrument procurement, branded packaging, and regulatory labeling, to fully documented export delivery — all under one managed relationship with a named point of contact.
Branded packaging — custom boxes, inserts, and sterilization pouches carrying your logo, product name, and catalogue codes — is coordinated alongside regulatory labeling, including UDI compliance for FDA-regulated markets and CE mark requirements for European distribution.
WHY BRAND BUILDERS CHOOSE US
Bio Tech Globals owns your entire OEM program – specification, instrument procurement, branded packaging, compliance labeling, and export clearance -under one managed relationship.
No instruments are marked, packaged, or prepared for export until your branded artwork – logos, regulatory labels, and catalogue codes – has been formally reviewed and approved in writing by your team.
Custom packaging — branded boxes, instrument inserts, and sterilization pouches carrying your logo, product name, and catalogue codes — is coordinated to your exact artwork specification.
Branded OEM programmes are accessible from 500 units per product line – a threshold designed for brands entering new instrument categories or distributors launching a first private-label range without committing to volumes that exceed their initial market plan.
FDA-regulated US distribution and EU MDR-compliant European markets each require specific regulatory labeling standards – including UDI compliance and CE mark declarations – we manage this.
Every OEM and private-label programme we manage is treated as commercially confidential – your brand identity, instrument specifications, and programme structure are not shared with other clients
OEM OPERATIONS
OEM PROGRAMME CREDENTIALS
HOW YOUR PROGRAMME RUNS
Share your instrument requirements, target markets, volume, and brand assets — logos, label artwork, packaging specifications, and regulatory compliance requirements for your distribution markets.
Your instrument specification, OEM surgical instrument configurations, branded artwork, and compliance labeling requirements are confirmed and locked before pricing, once you approve we move further.
Instruments are produced, marked to your specification, and packaged in your branded materials through coordinated Sialkot facilities — each stage verified against your locked programme specification.
Your branded instruments are cleared through export with a complete documentation pack – commercial invoice, compliance declarations and your OEM programme QC report – for every destination market in your order.