OEM & PRIVATE LABEL

Your OEM Surgical Instrument Program, Managed Under Your Brand

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

Your Brand Name on Compliant Instruments, Export-Ready and Delivered

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. 

Discuss OEM Requirements →

WHY BRAND BUILDERS CHOOSE US

Your Brand Program Managed with Accountability, Not Just Access

End-to-End Program Ownership

Bio Tech Globals owns your entire OEM program – specification, instrument procurement, branded packaging, compliance labeling, and export clearance -under one managed relationship.

No Production Without Approval

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.

Branded Packaging, Fully Managed

Custom packaging — branded boxes, instrument inserts, and sterilization pouches carrying your logo, product name, and catalogue codes — is coordinated to your exact artwork specification.

OEM from 500 Units

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.

Labels Compliant by Market

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.

Full Program Confidentiality

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

Private Label. Produced. Packaged. Delivered Under Your Brand.

Stainless steel dermatome skin graft knife resting in custom red velvet lined wooden case with laser-marked branding
Custom laser engraved wooden presentation case with Bio Tech Surgical Instruments branding for OEM white label packaging

OEM PROGRAMME CREDENTIALS

The Operational Record Behind Every OEM Programme We Manage

Minimum OEM Unit Order
500
Minimum OEM Unit Order
3
Artwork Review Turnaround
48 hr
Client Sign-Off Required
100 %

HOW YOUR PROGRAMME RUNS

From Your Brand Brief to Branded, Cleared Delivery — Fully Managed

Brief and Brand Assets

Share your instrument requirements, target markets, volume, and brand assets — logos, label artwork, packaging specifications, and regulatory compliance requirements for your distribution markets.

Specification Lock and Quote

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.

Production and Branded Packaging

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.

Export and Branded Delivery

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.