Identity
- Trade Name
- Dryswab FDA UDI
- Generic Name
- General-purpose absorbent tip applicator/swab, single-use FDA UDI
- Device Name
- Dryswab, straight aluminium wire peel pouch, rayon FDA UDI
- Model / Reference
- N/a FDA UDI
- Description
- Dryswab, straight aluminium wire peel pouch, rayon FDA UDI
Identifiers
- Catalog Number
- MW151 FDA UDI
- Primary DI / UDI-DI
- 05060259073120 FDA UDI
- FDA Product Code
- KCJ FDA UDI
- GMDN Term
- General-purpose absorbent tip applicator/swab, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.5220 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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: General-purpose absorbent tip applicator/swab, single-use
Dryswab by Medical Wire & Equipment Company (Bath), Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Medical Wire & Equipment Company (Bath), Ltd.
Sources (1)
- FDA UDI 39ba81ee-540a-40d7-9f26-14887357da9a 35 fields · synced May 30, 2026