FDA UDI In Commercial Distribution 🇺🇸 United States

NIPRO SCALP VEIN SET

DI: 00383790002509 · Model: PR+22G19 · NIPRO MEDICAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NIPRO SCALP VEIN SET
Primary DI
00383790002509
Version / Model
PR+22G19
Company Name
NIPRO MEDICAL CORPORATION
Labeler DUNS
797372554
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
d8c1102e-f523-4f93-a23f-769a691af197

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
35211 Scalp vein needle

Identifiers

Type ID
Package 40383790002507
Package 10383790002506
Primary 00383790002509

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Needle Gauge : 22 Gauge
Device Size Text, specify Tubing Length : 12 Inch
Device Size Text, specify NeedleLength : 3/4 Inch