FDA device listing
APEX BIOPSY PUNCH, 20CM,Baby Tischler, 20 cm Shaft, Straight, 2.3 x 4.2mm Bite,Baby Tischler Biopsy Forceps,Berger…
FDA device listing 2016640075 · Biopsy Fine Cut Instruments
Key facts
| Proprietary names | APEX BIOPSY PUNCH, 20CM,Baby Tischler, 20 cm Shaft, Straight, 2.3 x 4.2mm Bite,Baby Tischler Biopsy Forceps,Berger Biopsy Forceps,Burke Biopsy Forceps,Cushing Pituitary Rongeur, 5 (12.7 cm) Shaft, 2 x 10 mm Cup Jaws, Curved-Up,Douay Biopsy Forceps,Eppendorfer Biopsy Forceps,Faure Biopsy Forceps,Forceps, Biopsy, Gynecological,Kevorkian Biopsy Forceps,KEVORKIAN BIOPSY PUNCH, 20CM,Kevorkian Pacific… |
|---|---|
| Owner/operator | Biopsy Fine Cut Instruments |
| Owner/operator number | 10024093 |
| Product codes | HFB |
| Device names | HFB - Forceps, Biopsy, Gynecological |
| Device class | Class I |
| Classification regulations (21 CFR) | 884.4530 |
| Review panels | Obstetrics/Gynecology |
| Registered establishments | Biopsy Fine Cut Instruments |
| Establishment registrations | 3006891796 |
| FEI numbers | 3006891796 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database