FDA UDI In Commercial Distribution 🇺🇸 United States

Indigo System

DI: 00815948022591 · Model: LITNG12XTORQ115-A · PENUMBRA, INC.
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Indigo System
Primary DI
00815948022591
Version / Model
LITNG12XTORQ115-A
Company Name
PENUMBRA, INC.
Labeler DUNS
191077671
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-15
Public Version
4
Public Version Date
2022-11-09
Public Version Status
Update
Public Device Record Key
52c7faa2-b6c6-4cb9-aa63-c03fa5e32911

Device Description

CAT12 115 New XTORQ shape plus Lightning

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
Yes
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
QEW Peripheral Mechanical Thrombectomy With Aspiration

GMDN Terms

Code Name
58173 Thrombectomy suction catheter
16779 Suction/irrigation tubing, single-use

Identifiers

Type ID
Primary 00815948022591

Premarket Submissions

Submission Number Supplement Number
K192981 000
K193244 000