Identity
- Trade Name
- Quick-Core FDA UDI
- Generic Name
- Ultrasound aspiration biopsy procedure kit FDA UDI
- Device Name
- Quick-Core, Endoscopic Ultrasound Biopsy Needle FDA UDI
- Model / Reference
- G25507 FDA UDI
- Description
- Quick-Core, Endoscopic Ultrasound Biopsy Needle FDA UDI
Identifiers
- Catalog Number
- EUSN-19-QC FDA UDI
- Primary DI / UDI-DI
- 00827002255074 FDA UDI
- FDA Product Code
- FCG FDA UDI
- GMDN Term
- Ultrasound aspiration biopsy procedure kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1075 FDA UDI
- Commercial Distribution
- Not 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
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Quick-Core by Cook Ireland, Ltd. — 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
- Cook Ireland, Ltd.
Sources (1)
- FDA UDI 987ad40b-c82d-4768-a114-f2d374572d4b 37 fields · synced May 30, 2026