FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10841983101608 · Model: YG-922P · NIHON KOHDEN AMERICA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
NA
Primary DI
10841983101608
Version / Model
YG-922P
Catalog Number
YG-922P
Company Name
NIHON KOHDEN AMERICA, INC.
Labeler DUNS
021063219
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-09-19
Public Version
6
Public Version Date
2023-08-17
Public Version Status
Update
Public Device Record Key
ef249fb7-bc57-4e88-a620-499d760643ad
Distribution End Date
2023-08-03

Device Description

Water trap N-Neonate

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
CCK ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE

GMDN Terms

Code Name
33586 General-purpose multi-parameter bedside monitor

Identifiers

Type ID
Primary 10841983101608
Unit of Use 00841983101601

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Neonatal