FDA UDI In Commercial Distribution 🇺🇸 United States

Phoenix

DI: 44900719317014 · Model: PP2225G500-INT · DR.JAPAN CO., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
Phoenix
Primary DI
44900719317014
Version / Model
PP2225G500-INT
Company Name
DR.JAPAN CO., LTD.
Labeler DUNS
701082349
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2023-12-04
Public Version Status
Update
Public Device Record Key
9d092c86-65e7-423e-b987-dac1d67e4ca1

Device Characteristics

Single Use
Yes
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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
BSP Needle, Conduction, Anesthetic (W/Wo Introducer)

GMDN Terms

Code Name
35212 Spinal needle, single-use

Identifiers

Type ID
Primary 44900719317014
Unit of Use 04900719317016

Device Sizes

Type Value Unit Text
Length 5 Inch
Device Size Text, specify Tapers from 22 Gauge to 25 Gauge