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BOEHRINGER LABORATORIES, LLC

Last updated September 17, 2026

Information

Country: US
Address: 300 Thoms Drive, Phoenixville, PA, 19460
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Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 2518417
DUNS Number: —

Catalogue (157)

Page 1 of 4

Device	Model / Reference	Registries	Class	Status
BOEHRINGER® Replacement Gauge, 0-200mmHg	9071	FDA UDI	Class II	Active
BOEHRINGER® Suction Regulator CASS Continuous, 0-60, off/reg/pulse	3820	FDA UDI	Class II	Unknown
BOEHRINGER® Medstar/Oxequip Adapter	1498	FDA UDI	Class II	Active
BOEHRINGER® Lens Cap for 3800 Series, Colored Magenta	9066	FDA UDI	Class II	Active
BOEHRINGER® Arm Restraint Straps ( 1 pair ) - 27 Inches	9008	FDA UDI	Class I	Active
BOEHRINGER® Replacement Plastic Bottle for 9101 Trap	34059	FDA UDI	Class II	Active
BOEHRINGER® Lens Cap for 3800 Series, Colored Green	9065	FDA UDI	Class II	Active
BOEHRINGER® Regulator Washer	7992	FDA UDI	Class II	Unknown
BOEHRINGER® Replacement Vacuum Valve for 9101 Trap	34045	FDA UDI	Class II	Active
BOEHRINGER® Y Connector	2098	FDA UDI	Class II	Active
BOEHRINGER® Offset Mount - Four Inches	9061	FDA UDI	Class II	Active
BOEHRINGER® British Fitting	1511	FDA UDI	Class II	Unknown
BOEHRINGER® DIN Adapter	1499	FDA UDI	Class II	Active
BOEHRINGER® AUTOVAC® Modular Collection Module with Disconnect	792600	FDA UDI	Class II	Unknown
BOEHRINGER® ViSiGi 3D™ Calibration System for Roux-en-y, size 32Fr w/bulb	5232B	FDA UDI	Class II	Active
BOEHRINGER® CareDry™ Wand	7640	FDA UDI	Class II	Unknown
BOEHRINGER® CareDry™ Regulator	7620	FDA UDI	Class II	Unknown
BOEHRINGER® 1/8 NPT M-F-F Fitting	3946	FDA UDI	Class II	Unknown
TruLim Length Indicating Device	5010	FDA UDI	Class I	Unknown
BOEHRINGER® Elbow, 45 degrees	2468	FDA UDI	Class II	Active
Boehringer® Vavd Horizontal Mount	3944	FDA UDI	Class II	Unknown
BOEHRINGER® Lens Cap for 3800 Series, Colored Baby Blue	9076	FDA UDI	Class II	Active
BOEHRINGER® IV Pole Bracket	9086	FDA UDI	Class II	Unknown
BOEHRINGER® WAGD Replacement Hose	3947	FDA UDI	Class II	Active
BOEHRINGER® Valve, Shutoff w/ Y-Connector & Barb	7622	FDA UDI	Class II	Unknown
BOEHRINGER® High Flow Bubble Barb	2469	FDA UDI	Class II	Active
BOEHRINGER® ViSiGi 3D™ Low Suction Sleeve Gastrectomy Calibration Sys, size 36Fr	5236LS	FDA UDI	Class II	Unknown
BOEHRINGER® ViSiGi™ 3D Sleeve Gastrectomy Calibration System, size 40Fr	5240	FDA UDI	Class II	Active
BOEHRINGER® Disposable Regulator 100-150mmHg	7650	FDA UDI	Class II	Unknown
BOEHRINGER® ViSiGi 3D® Calibration System size 32Fr Bypass/Short w/bulb	5232SB	FDA UDI	Class II	Active
BOEHRINGER® 1/8" PVC Drain & Trocar	2062	FDA UDI	Class II	Unknown
BOEHRINGER® Oxequip Adapter	1497	FDA UDI	Class II	Active
BOEHRINGER® ViSiGi 3D® Calibration System size 36Fr Bypass/Short w/bulb	5236SB	FDA UDI	Class II	Active
BOEHRINGER® VAVD VacPac	3948	FDA UDI	Class II	Active
BOEHRINGER® SUPPLY LINE-VAVD-DIAMOND (20' length)	3941	FDA UDI	Class II	Unknown
BOEHRINGER® PHOENIX™ Containment System 12CM	5501	FDA UDI	Class II	Unknown
BOEHRINGER® ViSiGi 3D® Calibration System size 40Fr Bypass/Short w/bulb	5240SB	FDA UDI	Class II	Active
BOEHRINGER® Suction Regulator, MRI Conditional & Safe Continuous, 0-200, off/reg	3708	FDA UDI	Class II	Active
BOEHRINGER® ViSiGi Lux 40 Fr	5340SB	FDA UDI	Class II	Active
BOEHRINGER® CareConnect™ External Female Catheter Regulator	7620	FDA UDI	Class II	Unknown
BOEHRINGER® CareDry™ Male System	7680	FDA UDI	Class I	Active
BOEHRINGER® Full Line Valve	7693	FDA UDI	Class II	Unknown
BOEHRINGER® AUTOVAC® 792600 with 1/8" (10Fr) PVC Drain & Trocar	792612	FDA UDI	Class II	Unknown
BOEHRINGER® CareDry™ System	7660	FDA UDI	Class I	Active
BOEHRINGER® ViSiGi 3D® Calibration System size 40Fr Bypass/Short	5240S	FDA UDI	Class II	Active
BOEHRINGER® Safety Trap Bottle Stand Alone	9075	FDA UDI	Class II	Unknown
BOEHRINGER® ViSiGi 3D® Calibration System size 36Fr Bypass/Short	5236S	FDA UDI	Class II	Active
BOEHRINGER® Replacement Gauge, 0-760mmHg	9073	FDA UDI	Class II	Unknown
BOEHRINGER® Pipe Nipple 1/8" X 1 1/2	33291	FDA UDI	Class II	Active
BOEHRINGER® Smoke Removal System	5700	FDA UDI	Class I	Unknown

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FDA Recalls (6)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Aug 1, 2005	Z-0157-06	—	terminated	Condition exists that prevents complete shutoff of the valve
Aug 1, 2005	Z-0156-06	—	terminated	Condition exists that prevents complete shutoff of the valve
Aug 1, 2005	Z-0155-06	—	terminated	Condition exists that prevents complete shutoff of the valve
May 19, 2004	Z-1232-04	—	terminated	The suction regulator incorporates a gauge for the verification of suction levels. The particular lot of gauges used in the production of the regulators exhibits a potential to develop a leak and cause the delivered suction to be inaccurate.
May 19, 2004	Z-1231-04	—	terminated	The suction regulator incorporates a gauge for the verification of suction levels. The particular lot of gauges used in the production of the regulators exhibits a potential to develop a leak and cause the delivered suction to be inaccurate.
Nov 7, 2003	Z-0227-04	—	terminated	Inadequate bond where the tube attaches to the inlet of the bulb.