FDA UDI In Commercial Distribution 🇺🇸 United States

NIPRO BIOHOLE NEEDLE WITH CAPICK SCAB REMOVER

DI: 00383790001243 · Model: 15GX1" HC-30W-D-CAP · NIPRO MEDICAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NIPRO BIOHOLE NEEDLE WITH CAPICK SCAB REMOVER
Primary DI
00383790001243
Version / Model
15GX1" HC-30W-D-CAP
Catalog Number
FD+152530BC-CAP
Company Name
NIPRO MEDICAL CORPORATION
Labeler DUNS
797372554
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-01
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
7673753e-9a1b-4867-96a5-d1a31970b91d

Device Description

DULL FISTULA NEEDLE for Established Access Sites Only 15Gx1" Fixed Hub 12" Tubing

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FIE Needle, fistula

GMDN Terms

Code Name
12741 Haemodialysis needle

Identifiers

Type ID
Package 40383790001241
Package 10383790001240
Primary 00383790001243