Identity
- Trade Name
- A.T.T.S SILO FDA UDI
- Generic Name
- Surgical suction system collection container, reusable FDA UDI
- Device Name
- A.T.T.S. SILO FDA UDI
- Model / Reference
- 19-7900 FDA UDI
- Description
- A.T.T.S. SILO FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00851314007410 FDA UDI
- FDA Product Code
- KDQ FDA UDI
- GMDN Term
- Surgical suction system collection container, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Commercial Distribution
- Not 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
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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
A.t.t.s Silo by Innovative Med, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Innovative Med, Inc.
Sources (1)
- FDA UDI 752a8e0a-6bf9-4787-a2f7-db0e49e71c16 35 fields · synced May 30, 2026