Product Description
What this product is and who it is for
- The Welch Allyn Connex ProBP 3400 is a clinical spot‑check digital non‑invasive blood pressure device intended for outpatient and inpatient clinical settings. It is intended for users who need a mobile, stand‑mounted vital‑signs device that integrates with wired EHR/EMR systems.
Specifications
- Technology options: Standard NIBP or SureBP (fast measurement mode); this listing is for the 3400 series in the mobile‑stand configuration.
- Display: color graphical display (240 × 320 pixels, 16‑bit color).
- Pressure and measurement ranges: cuff pressure 0–300 mmHg; systolic 60–250 mmHg; diastolic 30–160 mmHg; MAP ≈ 40–190 mmHg.
- Cuff compatibility: Works with Welch Allyn FlexiPort cuff sizes 8 through 13 (small child to thigh).
- Power: rechargeable lithium‑ion battery; manufacturer-stated capacity up to ~100 readings per full charge.
- Connectivity: USB wired interface for integration to select EHR/HIS/EMR systems; Bluetooth is an optional upgrade on some SKUs.
What is included
- Device head (Connex ProBP 3400) mounted to a mobile stand with basket and five‑leg caster base (mobile‑stand configuration).
- Two FlexiPort cuffs shipped standard: size 11 (adult) and size 12 (large adult).
- BP tubing, rechargeable lithium‑ion battery, and a North America IEC power cord (final power‑cord suffix "B" indicates NA cord on published REF numbers).
Condition and packaging
- Manufacturer product images and authorized reseller documentation show the device mounted on a mobile stand; packaging state for any given unit is not visible in the supplied photo and should be confirmed with the seller prior to purchase.
Usage notes
- Device can be configured for Standard NIBP or SureBP operation (SureBP is the faster mode in manufacturer documents).
- When integrating with an EHR/EMR via USB, allow time for any site-specific interface development and testing.
- Not intended for neonatal use; do not use on neonates.
Limitations and incompatibilities
- Bluetooth wireless capability is not present on every SKU — confirm the exact REF/MPN if wireless is required.
- This device is not intended for neonatal use.
Regulatory and safety notes
- Manufacturer documentation and regulatory records indicate a customer medical device correction (recall/FSCA) was issued; buyers operating in regulated environments should confirm applicability and remediation with Welch Allyn/Hillrom before deploying.
Warnings
- Exact accessories and regional power‑cord variants depend on the SKU/MPN; verify included accessories with the seller.
- Photographs do not show retail packaging; the product may be shipped in bulk or manufacturer packaging depending on distributor.
