FDA UDI In Commercial Distribution 🇺🇸 United States

NIPRO SYRINGE

DI: 00383790011976 · Model: JD+10L2138 · NIPRO MEDICAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
NIPRO SYRINGE
Primary DI
00383790011976
Version / Model
JD+10L2138
Company Name
NIPRO MEDICAL CORPORATION
Labeler DUNS
797372554
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-01
Public Version
1
Public Version Date
2025-06-09
Public Version Status
New
Public Device Record Key
8333aea4-a20c-48be-850f-3ee415257cdf

Device Description

Syringe 10mL Luer Lock with Needle 21G x 1-1/2"

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
FMF Syringe, piston

GMDN Terms

Code Name
47017 General-purpose syringe, single-use

Identifiers

Type ID
Package 10383790011973
Primary 00383790011976
Package 40383790011974

Customer Contacts