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Keystone ASP Oropharyngeal Sterile Specimen Collection Swab 5000 pcs
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Keystone ASP Oropharyngeal Sterile Specimen Collection Swab 5000 pcs FDA UDI
- Generic Name
- General-purpose absorbent tip applicator/swab, single-use FDA UDI
- Device Name
- ASP Oropharyngeal Sterile Specimen Collection Swab 5000 pcs FDA UDI
- Model / Reference
- KMSWAB-ASPN-5000 FDA UDI
- Description
- ASP Oropharyngeal Sterile Specimen Collection Swab 5000 pcs FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860003793787 FDA UDI
- FDA Product Code
- KXG FDA UDI
- GMDN Term
- General-purpose absorbent tip applicator/swab, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6025 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
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: General-purpose absorbent tip applicator/swab, single-use
Keystone ASP Oropharyngeal Sterile Specimen Collection Swab 5000 pcs by Keystone Manufacturing — Class I — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as General-purpose absorbent tip applicator/swab, single-use.
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- ESCOB.FLOCK NASOF. 80MM FLOW — Deltalab, S.L. · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Keystone Manufacturing
Sources (1)
- FDA UDI 3e7743ae-7ab3-4d75-bc0d-d8d912bfb929 33 fields · synced May 31, 2026