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Canadian Hospital Specialties Limited

Last updated May 24, 2026

What Canadian Hospital Specialties Limited makes

Canadian Hospital Specialties Limited manufactures single-use and reusable medical devices for oxygen delivery, intravenous administration, enteral feeding, and diagnostic imaging. Their portfolio includes rebreathe masks, nasal cannulas, oral/enteral syringes, intravenous tubing extensions, and nasogastric feeding tubes, as well as reusable emesis bowls and angiographic syringes. The company also produces vacuum hoses, tubing connectors, and specialized cannulas for medical procedures. Additional items like drain line adapters and diagnostic imaging-related accessories are part of their offerings.

The company’s devices are classified under FDA’s Class I, Class II, and Unclassified (U) categories and are listed in the FDA’s Unique Device Identifier (UDI) database. These products are intended for use in clinical, hospital, and diagnostic settings in the United States. The manufacturer operates from a base in the US, adhering to applicable regulatory requirements for medical devices in that jurisdiction.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country: US
Address: —
Website: chsltd.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: 9058259300
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 240992693

Catalogue (324)

Page 3 of 7

Device	Model / Reference	Registries	Class	Status
Med-Rx	54-1650R	FDA UDI	Class II	Active
Corrugated Tubing	R-4026	FDA UDI	Class I	Active
Pediatric Nebulizer Kit	R-6920S	FDA UDI	Class I	Active
Aerosol Hood	R-2321	FDA UDI	Class I	Active
Infant Nasal Cannula - Vinyl	R-1301S	FDA UDI	Class I	Active
Med-Rx	54-7059	FDA UDI	Class II	Active
Steris	FL2107	FDA UDI	Class I	Active
Storz	20400162S	FDA UDI	Class II	Active
Med-Rx	YM54-5160	FDA UDI	Class I	Active
Med-Rx	10-1022	FDA UDI	Class II	Active
Oxygen Wrench	R-3040	FDA UDI	Class I	Active
Chs	T2020-G	FDA UDI	Class I	Active
Adult Nasal Cannula-vinyl	R-1704S	FDA UDI	Class I	Active
Adult Nasal Cannula-Vinyl	R-1701SF	FDA UDI	Class I	Active
Med-Rx	54-5136R	FDA UDI	Class II	Active
Adult 3 IN 1 Mask	R-2155	FDA UDI	Class I	Active
MISI-Medical Imaging Solutions International	100502D	FDA UDI	Class II	Active
Med-Rx	54-7063	FDA UDI	Class II	Active
Chs	BP1006-G	FDA UDI	Class I	Active
Saflo Oxygen Supply Tube	R-1574	FDA UDI	Class I	Active
Saflo Oxygen Supply Tube	R-1576M	FDA UDI	Class I	Active
MISI-Medical Imaging Solutions International	400101	FDA UDI	Class II	Active
Chs	EM1001	FDA UDI	Class I	Active
Jemsdal	A-271	FDA UDI	Class I	Active
Saflo Oxygen Supply Tube	R-1540	FDA UDI	Class I	Active
Med-Rx	10-1260	FDA UDI	Class II	Active
Kraton	R-1510	FDA UDI	Class I	Active
Med-Rx	YM54-5230	FDA UDI	Class II	Active
Chs	RB1008	FDA UDI	Class I	Active
Tavish	R-7500	FDA UDI	Class I	Active
Chs	EM1002-M	FDA UDI	Class I	Active
Adult Vari-Vent Mask	R-2300S	FDA UDI	Class I	Active
Med-Rx	10-1227	FDA UDI	Class II	Active
Tubing Connector	R-2990	FDA UDI	Class I	Active
Suture Removal Kit	8520	FDA UDI	Class I	Active
Saflo Oxygen Supply Tube	R-1573	FDA UDI	Class I	Active
Chs	WB1004-M	FDA UDI	Class I	Active
Chs	T2020-M	FDA UDI	Class I	Active
Med-Rx	54-5003	FDA UDI	Class II	Active
Med-Rx	54-2480R	FDA UDI	Class II	Active
Med-Rx	10-1041	FDA UDI	Class II	Active
Med-Rx	YM54-5120	FDA UDI	Class I	Active
Chs	C2021-G	FDA UDI	Class I	Active
MISI-Medical Imaging Solutions International	400302D	FDA UDI	Class II	Active
Med-Rx	54-1042R	FDA UDI	Class II	Active
Adult Non-Rebreathing Oxygen Mask	R-2460S	FDA UDI	Class I	Active
Neotech Ram Cannula™	N4901-NS	FDA UDI	Class I	Active
Neotech Ram Cannula™	N4905-NS	FDA UDI	Class I	Active
Chs	SB1005-G	FDA UDI	Class I	Active
Med-Rx	54-5201	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (5)

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

Canadian Hospital Specialties Limited has five FDA recall records initiated between June 11, 2018, and June 11, 2024. The records include one classified, one open, and three terminated cases, with reasons involving product packaging inconsistencies, incomplete seals potentially compromising sterility, detached connectors, and illegible barcodes on labels. Complaints were validated or reported by customers regarding deviations from labeled specifications, including incorrect tube lengths and scanning issues.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Jun 11, 2024	Z-2408-2024	—	open, classified	A customer found product with incomplete seals of P/N 20400161S, lot #185198 which can lead to non-sterile product and patient safety concerns. CHS has validated this complaint.
Aug 19, 2022	Z-0202-2023	—	terminated	Some of the labels of the kits for product code 10-4001 in the specified lots have an illegible barcode which prevents successful scanning of the package.
Jul 16, 2019	Z-2281-2019	—	terminated	The firm received a complaint that the connector detached from the feeding tube.
Dec 1, 2018	Z-0725-2019	—	terminated	The product may be packaged with a 5FR X 24 length Feeding tube instead of a 6.5 FR X 24 Feeding tube as labeled.
Jun 11, 2018	Z-2440-2018	—	terminated	The product may be packaged with the incorrect length of feeding tube as labeled.

FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

Canadian Hospital Specialties Ltd. MISSISSAUGA Ontario · CA FEI 3000153466