FDA Registration Active 🇯🇵 Japan

AG-920RA Mulitgas Unit

Reg #: 3007962724 · FEI: 3007962724 · Expires 2025
Products
8
Proprietary Names
2
Establishment Types
1
Classifications
8

Registration Details

Registration Name
Nihon Kohden Tomioka Corporation
Registration Number
3007962724
FEI Number
3007962724
Status
Active
Expiry Year
2025
Initial Importer
No
Address
486 Nanokaichi
City
Gunma Tokyo
Country
JP

Regulatory Submissions

510(k) Number
K020046

Owner / Operator

Firm Name
NIHON KOHDEN CORP.
Operator Number
8030227
Address
1-31-4 NISHIOCHIAI, SHINJUKU-KU
City
TOKYO
State
JP-13
Postal Code
161-8560
Country
JP

US Agent

Business Name
NIHON KOHDEN AMERICA, LLC.
Contact Name
Charlemagne Chua
Address
15353 Barranca Pkwy, --
City
Irvine
State
CA
ZIP
92618
Country
US
Phone
949 3303964

Products

Device Name Product Code
Analyzer, Gas, Halothane, Gaseous-Phase (Anesthetic Conc.) CBS
Analyzer, Gas, Isoflurane, Gaseous-Phase (Anesthetic Concentration) NHQ
Analyzer, Gas, Sevoflurane, Gaseous-Phase (Anesthetic Concentration) NHP
Analyzer, Gas, Oxygen, Gaseous-Phase CCL
Analyzer, Gas, Enflurane, Gaseous-Phase (Anesthetic Concentration) CBQ
Analyzer, Gas, Nitrous-Oxide, Gaseous Phase (Anesthetic Conc.) CBR
Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase CCK
Analyzer, Gas, Desflurane, Gaseous-Phase (Anesthetic Concentration) NHO

Proprietary Names

AG-920RA Mulitgas Unit AG-920RA

Establishment Types

Manufacture Medical Device