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Canadian Hospital Specialties Limited

US

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
—
Phone
9058259300
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
240992693

Catalogue (324)

Page 2 of 7
DeviceModel / ReferenceRegistriesClassStatus
Med-Rx 10-4001
FDA UDI
Class IIActive
Med-Rx 10-1014A
FDA UDI
Class IIActive
Pediatric Non-Rebreathing Oxygen Mask R-2960S
FDA UDI
Class IActive
Key Surgical FL-2010
FDA UDI
Class IActive
Chs BP1006-TEAL
FDA UDI
Class IActive
Chs S2011-CL
FDA UDI
Class IActive
Kraton R-1400S
FDA UDI
Class IActive
Med-Rx 54-5001
FDA UDI
Class IIActive
Med-Rx 10-1026
FDA UDI
Class IIActive
Med-Rx 54-5220
FDA UDI
Class IIActive
Adult Non-rebreathing Oxygen Mask R-2450S
FDA UDI
Class IActive
Med-Rx 10-1021A
FDA UDI
Class IIActive
Chs WB1004-G
FDA UDI
Class IActive
Med-Rx 54-1204
FDA UDI
Class IIActive
Med-Rx 70-8180
FDA UDI
Class IIActive
Med-Rx 10-1353
FDA UDI
Class IActive
VixOne™ Nebulizer Kit R-6405S
FDA UDI
Class IActive
Chs S2009
FDA UDI
Class IActive
Wilburn Medical USA WUSA/6013
FDA UDI
Class IIActive
Adult Oxygen Mask High Concentration R-2450SM
FDA UDI
Class IActive
Adult Nasal Cannula-Vinyl R-1701SM
FDA UDI
Class IActive
Med-Rx 54-7066
FDA UDI
Class IIActive
19mm Magenta Tubing Connector R-2980M
FDA UDI
Class IActive
Med-Rx 10-1020
FDA UDI
Class IIActive
Med-Rx 54-8142R
FDA UDI
Class IIActive
Tavish R-7450S
FDA UDI
Class IActive
Corrugated Tubing R-4020B
FDA UDI
Class IActive
Saflo Oxygen Supply Tube R-1576
FDA UDI
Class IActive
Chs 54-5005
FDA UDI
Class IActive
T-Piece R-6402
FDA UDI
Class IActive
Chs SBP1010-G
FDA UDI
Class IActive
Med-Rx 54-5003
FDA UDI
Class IIActive
Steris FL2010
FDA UDI
Class IActive
Steris FL2110
FDA UDI
Class IActive
Key Surgical FL-2407
FDA UDI
Class IActive
VixOne™ Nebulizer Kit R-6415S
FDA UDI
Class IActive
Pediatric Oxygen Mask R-2700S
FDA UDI
Class IActive
Med-Rx 54-5115R
FDA UDI
Class IIActive
Pediatric Non-rebreathing Oxygen Mask R-2950S
FDA UDI
Class IActive
Tavish R-7200S
FDA UDI
Class IActive
Chs SBP1010-M
FDA UDI
Class IActive
MISI-Medical Imaging Solutions International 400109
FDA UDI
Class IIActive
Adult Nebulizer Kit MS-6420S
FDA UDI
Class IActive
MISI-Medical Imaging Solutions International 400108
FDA UDI
Class IIActive
Neotech RAM CANNULA™ N4904-NS
FDA UDI
Class IActive
MISI-Medical Imaging Solutions International 100301T
FDA UDI
Class IIActive
MISI-Medical Imaging Solutions International 200105A
FDA UDI
Class IIActive
DeRoyal 77-3200
FDA UDI
Class IIActive
Med-Rx 10-1254
FDA UDI
Class IIActive
Tubing 7 Reinforced Saflo 014E4002
FDA UDI
Class IActive

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.

DateRecall No.ClassStatusReason
Jun 11, 2024Z-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, 2022Z-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, 2019Z-2281-2019—terminated

The firm received a complaint that the connector detached from the feeding tube.

Dec 1, 2018Z-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, 2018Z-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