Identity
- Trade Name
- Reusable Acoustic Standoff Pad FDA UDI
- Generic Name
- Diagnostic ultrasound phantom, anthropomorphic FDA UDI
- Device Name
- Reusable non-sterile (1 x 10 x 15cm) FDA UDI
- Model / Reference
- 610-459 FDA UDI
- Description
- Reusable non-sterile (1 x 10 x 15cm) FDA UDI
Identifiers
- Catalog Number
- 610-459 FDA UDI
- Primary DI / UDI-DI
- 00841436103718 FDA UDI
- 510(k) Number
- K992152 FDA UDI
- FDA Product Code
- ITX FDA UDI
- GMDN Term
- Diagnostic ultrasound phantom, anthropomorphic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1570 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Dimensions & Sizes
- Size
- Width — 10 Centimeter FDA UDILength — 15 Centimeter FDA UDI
Reusable Acoustic Standoff Pad by Civco Medical Instruments Co., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Civco Medical Instruments Co., Inc.
Sources (1)
- FDA UDI 674851bc-d9ed-4551-b9cd-2d61a6696391 39 fields · synced Jun 8, 2026