FDA UDI In Commercial Distribution 🇺🇸 United States

SPECTRE

DI: 10841156108014 · Model: IPN916605 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SPECTRE
Primary DI
10841156108014
Version / Model
IPN916605
Catalog Number
7386
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-15
Public Version
2
Public Version Date
2024-01-22
Public Version Status
Update
Public Device Record Key
6af54d5d-468c-46b0-a9be-bd3535da29e4

Device Description

Spectre Guidewire, 200cm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DQX Wire, guide, catheter

GMDN Terms

Code Name
35094 Cardiac/peripheral vascular guidewire, single-use

Identifiers

Type ID
Package 20841156108011
Primary 10841156108014

Customer Contacts

Device Sizes

Type Value Unit Text
Length 200 Centimeter