FDA UDI In Commercial Distribution 🇺🇸 United States

SPECTRE

DI: 10841156111410 · Model: IPN930527 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
SPECTRE
Primary DI
10841156111410
Version / Model
IPN930527
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
2025-06-04
Public Version
1
Public Version Date
2025-06-12
Public Version Status
New
Public Device Record Key
251a71b3-2e1e-439b-811c-46bf6821ba74

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
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 20841156111417
Primary 10841156111410

Customer Contacts