FDA UDI Not in Commercial Distribution 🇺🇸 United States

Neptune®

DI: 00816849019253 · Model: DNX-454 · ENDOCHOICE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

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Basic Information

Brand Name
Neptune®
Primary DI
00816849019253
Version / Model
DNX-454
Company Name
ENDOCHOICE, INC.
Labeler DUNS
014154279
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-09-08
Public Version
4
Public Version Date
2024-01-31
Public Version Status
Update
Public Device Record Key
a93a754e-8004-4970-b55a-4778f0f6bb8d
Distribution End Date
2024-01-30

Device Description

22 Gauge (0.7 mm) Injection Needle

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FBK Endoscopic Injection Needle, Gastroenterology-Urology

GMDN Terms

Code Name
38825 General-purpose endoscopic needle, single-use

Identifiers

Type ID
Primary 00816849019253
Unit of Use 00816849019246

Customer Contacts

Phone
888-632-3636

Device Sizes

Type Value Unit Text
Needle Gauge 22 Gauge