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Sign in to claim this brandCanadian 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
- —
- —
- [email protected]
- Phone
- 9058259300
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 240992693
Catalogue (324)
Page 1 of 7| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tavish | R-7950S | FDA UDI | Class I | Active |
| MISI-Medical Imaging Solutions International | 200101i | FDA UDI | Class II | Active |
| Corrugated Tubing | R-4000 | FDA UDI | Class I | Active |
| Swivel Tubing Connector | R-3000 | FDA UDI | Class I | Active |
| Neotech Ram Cannula | N4902-NS | FDA UDI | Class I | Active |
| Safety Drain line adapter | M7010 | FDA UDI | Class I | Active |
| Med-Rx | 10-1040 | FDA UDI | Class II | Active |
| Med-Rx | 54-3665R | FDA UDI | Class II | Active |
| Med-Rx | 70-8240 | FDA UDI | Class II | Active |
| Jemsdal | A-221 | FDA UDI | Class I | Active |
| Med-Rx | YM54-5050 | FDA UDI | Class I | Active |
| Smart Scale | 56360 | FDA UDI | Class I | Active |
| Wilburn Medical USA | WUSA/0403 | FDA UDI | Class II | Active |
| Chs | S6001 | FDA UDI | Class I | Active |
| Med-Rx | 54-2440R | FDA UDI | Class II | Active |
| Kraton | R-1500SF | FDA UDI | Class I | Active |
| Respan | R-7420S | FDA UDI | Class I | Active |
| Respiratory Anesthesia Connector – Catheter Mount | 95003204 | FDA UDI | Class I | Active |
| VixOne™ Nebulizer Kit | R-6400 | FDA UDI | Class I | Active |
| Non-breathing Oxygen Mask with 7FT Saflo Oxygen Supply Tubing | MS-2960S | FDA UDI | Class I | Active |
| Tavish | R-9950S | FDA UDI | Class I | Active |
| Small Adult 3 In 1 Mask | R-8155 | FDA UDI | Class I | Active |
| Chs | S5000-O | FDA UDI | Class I | Active |
| Pediatric Oxygen Mask | R-2700SM | FDA UDI | Class I | Active |
| Med-Rx | 54-5210 | FDA UDI | Class II | Active |
| Oxygen Wrench | VA-3040 | FDA UDI | Class I | Active |
| Pediatric Non-Rebreathing Oxygen Mask | R-2950SM | FDA UDI | Class I | Active |
| Med-Rx | 10-1257 | FDA UDI | Class II | Active |
| Chs | S4000 | FDA UDI | Class I | Active |
| Med-Rx | 10-1358 | FDA UDI | Class I | Active |
| Security Chain | R-3030 | FDA UDI | Class I | Active |
| Med-Rx | YM54-5110 | FDA UDI | Class I | Active |
| Storz | 20400161S | FDA UDI | Class II | Active |
| MISI-Medical Imaging Solutions International | 100501S | FDA UDI | Class II | Active |
| PPE CPAP Smoothbore Tubing | R-4420-72/50 | FDA UDI | Class I | Active |
| Chs | BP4230-M | FDA UDI | Class I | Active |
| Chs | R-2800SM | FDA UDI | Class I | Active |
| Swivel Tubing Connector | R-3000/25 | FDA UDI | Class I | Active |
| Chs | S2012-M | FDA UDI | Class I | Active |
| Saflo Oxygen Supply Tube | R-1575 | FDA UDI | Class I | Active |
| Nebulizer Kit | MS-6920S | FDA UDI | Class I | Active |
| Adult High Concentration Oxygen Mask with 7’ Saflo Tube | R-2250S | FDA UDI | Class I | Active |
| Wilburn Medical USA | WUSA/COMBO | FDA UDI | Class II | Active |
| Corrugated Tubing | R-4000-6 | FDA UDI | Class I | Active |
| Med-Rx | 54-3650R | FDA UDI | Class II | Active |
| Med-Rx | YM54-5105 | FDA UDI | Class I | Active |
| Pediatric Aerosol Mask | R-2921S | FDA UDI | Class I | Active |
| Med-Rx | 10-4000 | FDA UDI | Class II | Active |
| Med-Rx | 10-1304 | FDA UDI | Class II | Active |
| Chs | UC1007PS | FDA UDI | Class I | 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