Identity
- Trade Name
- EBA2 FDA UDI
- Generic Name
- Pass-through cabinet FDA UDI
- Model / Reference
- Box for screws FDA UDI
Identifiers
- Catalog Number
- EBA-0350 FDA UDI
- Primary DI / UDI-DI
- 08032909627691 FDA UDI
- 510(k) Number
- K131005 FDA UDI
- FDA Product Code
- HSB FDA UDI
- GMDN Term
- Pass-through cabinet FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3020 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
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Pass-through cabinet
Eba2 by Citieffe — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Pass-through cabinet.
Cleared under the same submission
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
- Citieffe
Sources (1)
- FDA UDI 4f4df8d9-dd22-432e-b3b0-cc7991e20547 36 fields · synced May 30, 2026