FDA UDI In Commercial Distribution 🇺🇸 United States

Lehman™

DI: 00763000199043 · Model: 001259 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Lehman™
Primary DI
00763000199043
Version / Model
001259
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-02-03
Public Version
1
Public Version Date
2019-03-06
Public Version Status
New
Public Device Record Key
58f5f8e0-0d85-4967-88a3-752374136715

Device Description

WVN CATH 001259 10PK 6F 100 LEHMAN

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC

GMDN Terms

Code Name
10688 Angiographic catheter, single-use

Identifiers

Type ID
Package 20763000199047
Primary 00763000199043

Customer Contacts

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 1.194 Millimeter
Catheter Gauge 6.0 French
Length 100.0 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store catheters in a cool, dry area.