FDA UDI In Commercial Distribution 🇺🇸 United States

NIPRO SAFETOUCH™ II SAFETY FISTULA NEEDLE

DI: 00383790000192 · Model: 17GX1" HTC-30W · NIPRO MEDICAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NIPRO SAFETOUCH™ II SAFETY FISTULA NEEDLE
Primary DI
00383790000192
Version / Model
17GX1" HTC-30W
Catalog Number
FS+172530BCR
Company Name
NIPRO MEDICAL CORPORATION
Labeler DUNS
797372554
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-20
Public Version
3
Public Version Date
2018-12-20
Public Version Status
Update
Public Device Record Key
546e2eb1-561c-4173-9589-e790fc7fa852

Device Description

17Gx1" Rotating Hub 11" 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
FOZ Catheter,intravascular,therapeutic,short-term less than 30 days

GMDN Terms

Code Name
12741 Haemodialysis needle

Identifiers

Type ID
Package 10383790000199
Primary 00383790000192
Package 40383790000190