CELSIUS Catheter 8 mm | REF SMAPRIV2

The CELSIUS Catheter 8 mm (REF SMAPRIV2) by Johnson & Johnson is a steerable diagnostic and radiofrequency (RF) ablation catheter engineered for use in cardiac electrophysiology procedures. Featuring an 8 mm distal tip electrode, the device is intended to support intracardiac signal recording, electrical stimulation, and the delivery of RF energy during catheter-based mapping and ablation workflows.

Key Features
- 8 mm distal tip electrode designed to support larger lesion creation during RF ablation
- Steerable, deflectable shaft for navigation within cardiac chambers
- Multiple electrodes for intracardiac electrogram recording and pacing
- Compatible with standard RF generators and recording systems used in EP labs
- Single-use, sterile-packaged configuration
- Manufactured by Biosense Webster, a Johnson & Johnson MedTech company

Clinical Applications
- Electrophysiological mapping of the heart
- Radiofrequency ablation of arrhythmogenic cardiac tissue
- Intracardiac pacing and stimulation during EP studies
- Use within hospital electrophysiology laboratories by trained physicians

Product Information
- Product: CELSIUS Catheter 8 mm
- REF/UPN: SMAPRIV2
- Brand: Johnson & Johnson (Biosense Webster)
- Category: EP Ablation Catheters
- Tip electrode: 8 mm
- Curve type / shaft length / French size: Not specified in the located sources
- Sterility: Provided sterile, single-use
- Regulatory status: Not specified in the located sources

REF / UPNSMAPRIV2
Size8 mm

How It Works

1

Submit Your Request

Tell us what product you need and share a few details.

2

We Match You

We connect your request with the most relevant verified brands.

3

Receive Offers

Relevant supplier options can respond with availability, documentation context, and quote details.

Buyer support

Frequently asked questions about CELSIUS Catheter 8 mm | REF SMAPRIV2

Practical answers for procurement teams reviewing this product page.

Include the exact product family, brand preference, REF/UPN code when available, required quantity, destination country, expected delivery timing and documentation expectations.

Yes. If alternatives are acceptable, mention equivalent brands, compatible models, size ranges and any non-negotiable requirements.

Related products are connected through structured catalog data such as brand, category, product family and country assignment.

No. This page supports sourcing and RFQ organization. Buyers must verify regulatory status, clinical suitability and procurement compliance independently.

Specific codes reduce ambiguity and help supplier teams identify product availability, packaging details and documentation faster.

Yes. The workflow is designed for hospitals, clinics, distributors, wholesalers, importers and procurement departments.

Yes. Products can be connected to multiple countries in the admin panel, and buyers can specify destination details in the RFQ form.

The request is stored with contact and procurement details so the sourcing conversation can be reviewed and followed up clearly.

Your request has been captured successfully.