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Sign in to claim this brandMCKESSON MEDICAL-SURGICAL INC.
US
Last updated May 23, 2026
What MCKESSON MEDICAL-SURGICAL INC. makes
The company manufactures single-use medical gloves—both nitrile and natural rubber latex varieties, without powder or antimicrobial coatings—alongside disposable surgical drapes and adhesive bandages. It also produces hypodermic needles, aneroid blood pressure cuffs, compression stockings, and indwelling urethral drainage catheters without antimicrobial treatments.
These products are classified under FDA’s Class I and Class II regulations, with some falling under the U (unclassified) designation, and are listed in the FDA’s UDI (Unique Device Identification) database. The manufacturer operates from the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does McKesson Medical-Surgical Inc. manufacture?
McKesson Medical-Surgical Inc. produces a range of single-use medical devices, including nitrile and natural rubber latex examination and treatment gloves (both non-powdered and non-antimicrobial), disposable surgical drapes, adhesive bandages, hypodermic needles, aneroid manual sphygmomanometers (blood pressure cuffs), compression stockings, and indwelling urethral drainage balloon catheters without antimicrobial coatings. These devices are designed for clinical, surgical, and patient care settings.
Where is McKesson Medical-Surgical Inc. based?
McKesson Medical-Surgical Inc. is headquartered in the United States. The company’s location is relevant for regulatory oversight, manufacturing standards, and compliance with U.S. medical device regulations.
Which regulatory registries list McKesson Medical-Surgical Inc.’s devices?
McKesson Medical-Surgical Inc.’s devices are listed in the FDA’s Unique Device Identification (UDI) database. This registry helps track and identify medical devices through standardized identifiers, ensuring transparency in the supply chain and regulatory compliance.
How are McKesson Medical-Surgical Inc.’s devices classified under FDA regulations?
McKesson Medical-Surgical Inc.’s devices fall under FDA’s Class I (low-risk, general controls), Class II (moderate-risk, requiring special controls), and U (Unclassified) categories. Classification depends on factors like intended use, potential risks, and regulatory history. For example, single-use gloves and adhesive bandages are typically Class I, while devices like indwelling catheters may require additional scrutiny under Class II or U.
Why do some of McKesson Medical-Surgical Inc.’s devices have a ‘U’ classification?
The ‘U’ classification (Unclassified) means these devices lack a predefined regulatory pathway under FDA’s existing Class I or II frameworks. This designation often applies to newer or less common devices where risk assessment hasn’t yet established standard controls. The FDA may later reclassify them based on post-market performance data or safety concerns, but they remain subject to general device regulations until then.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 023904428
Catalogue (3381)
Page 4 of 68| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| McKesson | 01-670HBKGM | FDA UDI | Class I | Active |
| McKesson | 30642000 | FDA UDI | Class I | Active |
| McKesson | 14-316 | FDA UDI | Class I | Active |
| McKesson | 16-40224 | FDA UDI | Class I | Active |
| McKesson | 26547 | FDA UDI | Class II | Active |
| McKesson | S8683GX | FDA UDI | Class II | Active |
| McKesson | 16-N221 | FDA UDI | Class II | Active |
| McKesson | 16-M1612C | FDA UDI | Class II | Active |
| McKesson | 63-4475 | FDA UDI | Class I | Active |
| McKesson | 1800P | FDA UDI | U | Unknown |
| McKesson | 16-L2TNWT6Y-OSFM | FDA UDI | Class I | Active |
| Cypress | 23-32 | FDA UDI | Class I | Active |
| CareStock | CS2592 | FDA UDI | Class I | Active |
| McKesson | MCKELV8T45-3 | FDA UDI | Class I | Active |
| McKesson | 16-9703 | FDA UDI | Class I | Active |
| McKesson | 159-Si-24 | FDA UDI | Class I | Active |
| McKesson | 16-3B-44 | FDA UDI | Class I | Active |
| McKesson | 16-1309 | FDA UDI | Class I | Active |
| McKesson | 37-6291 | FDA UDI | U | Active |
| McKesson | 43-1-431 | FDA UDI | Class I | Active |
| McKesson | 209 | FDA UDI | Class II | Active |
| McKesson | SJ494G | FDA UDI | Class II | Active |
| McKesson | 8558 | FDA UDI | Class I | Active |
| McKesson | 43-1-219 | FDA UDI | Class I | Active |
| McKesson | 170-74006 | FDA UDI | Class I | Active |
| McKesson | 14-32080 | FDA UDI | Class I | Active |
| McKesson | 16-6008-B | FDA UDI | Class II | Active |
| Cypress | 27-74 | FDA UDI | Class I | Unknown |
| McKesson | 16-INS05C2805PT | FDA UDI | Class II | Active |
| McKesson | 24-202 | FDA UDI | Class I | Active |
| McKesson | 1189482 | FDA UDI | Class II | Active |
| McKesson | 16-47310S | FDA UDI | Class I | Active |
| McKesson | 84-04M | FDA UDI | Class II | Active |
| McKesson | 14-6N56C | FDA UDI | Class I | Active |
| McKesson | 200-IVRB18116 | FDA UDI | Class II | Active |
| McKesson | 16-VOL2500 | FDA UDI | Class II | Active |
| McKesson | 4822 | FDA UDI | Class I | Active |
| McKesson | 6003 | FDA UDI | Class II | Active |
| McKesson | 16-BW5048 | FDA UDI | Class II | Active |
| McKesson | 43-1-877 | FDA UDI | Class I | Active |
| McKesson | 16-4817 | FDA UDI | Class I | Active |
| McKesson | 1882 | FDA UDI | Class I | Active |
| McKesson | 84-41 | FDA UDI | Class II | Active |
| McKesson | 711 | FDA UDI | Class I | Active |
| McKesson | 61-59420 | FDA UDI | U | Active |
| McKesson | 16-LFOL512 | FDA UDI | Class II | Active |
| McKesson | 01-776-MCE | FDA UDI | Class II | Active |
| Mckesson | 194-0123-12 | FDA UDI | Class II | Active |
| McKesson | 4930 | FDA UDI | U | Active |
| McKesson | 16-LC04-REFILL | FDA UDI | Class I | Active |
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