Identity
- Trade Name
- FABCO FDA UDI
- Generic Name
- Dry medical towel/wipe, single-use FDA UDI
- Device Name
- Instrument Wipe 1mm FDA UDI
- Model / Reference
- Q604201 FDA UDI
- Description
- Instrument Wipe 1mm FDA UDI
Identifiers
- Catalog Number
- Q604201 FDA UDI
- Primary DI / UDI-DI
- 30634303800237 FDA UDI
- FDA Product Code
- NAB FDA UDI
- GMDN Term
- Dry medical towel/wipe, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4014 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
Dimensions & Sizes
- Size
- Height — 1 Millimeter FDA UDIWidth — 8.25 Centimeter FDA UDILength — 8.25 Centimeter FDA UDI
Category: Dry medical towel/wipe, single-use
Fabco by First Aid Bandage Co Inc — 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
- First Aid Bandage Co Inc
Sources (1)
- FDA UDI ceba4dec-939a-428e-8c68-d5061ab7d401 36 fields · synced May 31, 2026