Identity
- Trade Name
- McKesson FDA UDI
- Generic Name
- Luer-formatted disinfection cap FDA UDI
- Device Name
- Cap, Disinfecting for Needle Free Valves, Strip of 10 FDA UDI
- Model / Reference
- 421-SCXT3-10-2000 FDA UDI
- Description
- Cap, Disinfecting for Needle Free Valves, Strip of 10 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 20612479261642 FDA UDI
- 510(k) Number
- K130975 FDA UDI
- FDA Product Code
- QBP FDA UDI
- GMDN Term
- Luer-formatted disinfection cap FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5440 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Luer-formatted disinfection cap
McKesson by Mckesson Medical-Surgical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Luer-formatted disinfection cap.
- RPC — Reprocessing Products Corp · Class I
- 3M™ Curos™ — 3M COMPANY · U
- Curos Tips™ — 3M COMPANY · U
- Curos Jet™ — 3M COMPANY · U
- ClearGuard™ — ICU MEDICAL, INC. · Class II
- Molded Products, Inc. — MOLDED PRODUCTS INC. · Class II
- ICU Medical — ICU MEDICAL, INC. · Class II
- SwabTip™ — ICU MEDICAL, INC. · Class II
Cleared under the same submission
K130975 also covers:
- SwabCap™ — ICU MEDICAL, INC.
- SwabCap™ — ICU MEDICAL, INC.
- SwabSleeve™ — ICU MEDICAL, INC.
- McKesson — MCKESSON MEDICAL-SURGICAL INC.
- Excelsior — MEDLINE INDUSTRIES, INC.
- Excelsior — MEDLINE INDUSTRIES, INC.
- Excelsior — MEDLINE INDUSTRIES, INC.
- Excelsior — MEDLINE INDUSTRIES, INC.
- Excelsior — MEDLINE INDUSTRIES, INC.
- Excelsior — MEDLINE INDUSTRIES, INC.
- PENDING — MEDLINE INDUSTRIES, INC.
- PENDING — MEDLINE INDUSTRIES, INC.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Mckesson Medical-Surgical Inc.
Sources (1)
- FDA UDI 429d3e6c-65a4-4890-9e1c-387daf8fbdfb 34 fields · synced May 30, 2026