Identity
- Trade Name
- E-Z-GEL UltraSound Gel FDA UDI
- Generic Name
- Skin topical coupling gel FDA UDI
- Device Name
- EZ Gel 5L FDA UDI
- Model / Reference
- 601004 FDA UDI
- Description
- EZ Gel 5L FDA UDI
Identifiers
- Catalog Number
- 601004 FDA UDI
- Primary DI / UDI-DI
- 10815112021433 FDA UDI
- FDA Product Code
- MUI FDA UDI
- GMDN Term
- Skin topical coupling gel FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1570 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
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
Yes
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 5 Liter FDA UDI
Category: Skin topical coupling gel
E-Z-GEL UltraSound Gel by Bracco Diagnostics Inc. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Bracco Diagnostics Inc.
Sources (1)
- FDA UDI a9e6ba3b-fdae-4ea6-bb55-787470c341e0 36 fields · synced May 30, 2026