FDA Establishment Registration & Device Listing
U.S. Food & Drug Administration — Registered Establishment & Listed Device
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Establishment Registration & Device Listing
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FDA ESTABLISHMENT REGISTRATION & DEVICE LISTING
Proprietary Name
ToRR
Classification Name
ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
Product Code
GEI
Device Class
2
Regulation Number
878.4400
Medical Specialty
General & Plastic Surgery
Registered Establishment
| Establishment Name | BRITZMEDI CO., LTD |
|---|---|
| Establishment Number | 3029916132 |
| Premarket Submissions | K212561 |
Owner/Operator
| Owner/Operator | Britzmedi Co., Ltd |
|---|---|
| Owner/Operator Number | 10088936 |
| Establishment Operations | Contract Manufacturer |
Page Last Updated: 12/20/2024 — Source: FDA.gov Establishment Registration & Device Listing Database
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Page Footer & Navigation
This page contains FDA website navigation links and footer information from the official FDA.gov Establishment Registration & Device Listing database printout.
The listing confirms that BRITZMEDI CO., LTD (Establishment No. 3029916132) is a registered FDA establishment with the ToRR device (Product Code: GEI) under 510(k) number K212561.