FDA UDI In Commercial Distribution 🇺🇸 United States

Integra®

DI: 10381780072270 · Model: NL8501202 · Integra Lifesciences Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra®
Primary DI
10381780072270
Version / Model
NL8501202
Catalog Number
NL8501202
Company Name
Integra Lifesciences Corporation
Labeler DUNS
083171244
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-15
Public Version
6
Public Version Date
2023-05-16
Public Version Status
Update
Public Device Record Key
10bf92b2-5a42-40e0-b465-a7d7233706e5

Device Description

Integra® Pudenz Cardiac Catheter Barium Impregnated Stripe Radiopaque Tantalum Graduations

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
MR Conditional
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
JXG Shunt, central nervous system and components

GMDN Terms

Code Name
61158 Atrial cerebrospinal fluid catheter

Identifiers

Type ID
Primary 10381780072270
Secondary M269NL85012021

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Tubing: 1.3 mm ID x 2.2 mm OD; Total Length: 60 cm (23 1/2") (all dimensions nominal)

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
SpeciaAvoid contaminants such as lint, fingerprints, or talc.