FDA UDI In Commercial Distribution 🇺🇸 United States

NIPRO HYPODERMIC NEEDLE

DI: 00383790001908 · Model: AH+2025 · NIPRO MEDICAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
NIPRO HYPODERMIC NEEDLE
Primary DI
00383790001908
Version / Model
AH+2025
Catalog Number
AH+2025-1M
Company Name
NIPRO MEDICAL CORPORATION
Labeler DUNS
797372554
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
4
Public Version Date
2019-10-23
Public Version Status
Update
Public Device Record Key
bc550a6f-4a36-48d0-97b8-13c2a10c94c6

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
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMI Needle, Hypodermic, Single Lumen

GMDN Terms

Code Name
59230 Hypodermic needle, single-use

Identifiers

Type ID
Package 40383790001906
Package 20383790001902
Package 10383790001905
Primary 00383790001908

Customer Contacts

Device Sizes

Type Value Unit Text
Needle Gauge 20 Gauge
Length 1 Inch