Identity
- Trade Name
- UltraCore™ Biopsy Needle FDA UDI
- Generic Name
- End-cut biopsy gun needle FDA UDI
- Device Name
- UltraCore™ Biopsy Needle 18ga x 10cm FDA UDI
- Model / Reference
- 762618100 FDA UDI
- Description
- UltraCore™ Biopsy Needle 18ga x 10cm FDA UDI
Identifiers
- Catalog Number
- 762618100 FDA UDI
- Primary DI / UDI-DI
- 00886333006465 FDA UDI
- FDA Product Code
- DWO FDA UDI
- GMDN Term
- End-cut biopsy gun needle FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- 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
Category: End-cut biopsy gun needle
UltraCore™ Biopsy Needle by Argon Medical Devices, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as End-cut biopsy gun needle.
- FAST-CUT B — STERYLAB SRL · Class II
- Palium Needle — M.D.L. S.R.L. · Class I
- FAST-CUT B — STERYLAB SRL · Class II
- FAST-CUT B — STERYLAB SRL · Class II
- FAST-CUT — STERYLAB SRL · Class II
- Palium Needle — M.D.L. S.R.L. · Class I
- FastCutE — M.D.L. S.R.L. · Class I
- Palium Needle — M.D.L. S.R.L. · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Argon Medical Devices, Inc.
Sources (1)
- FDA UDI 60236ac3-6e4f-451a-ad91-10394855aed5 37 fields · synced Jun 9, 2026