FDA UDI In Commercial Distribution 🇺🇸 United States

TorqMax Sheath Grip Accessory

DI: 00813132020446 · Model: 502-001 · Spectranetics Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
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
TorqMax Sheath Grip Accessory
Primary DI
00813132020446
Version / Model
502-001
Catalog Number
502-001
Company Name
Spectranetics Corporation
Labeler DUNS
151047370
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-02-06
Public Version
7
Public Version Date
2024-08-21
Public Version Status
Update
Public Device Record Key
7417c4fa-d9a8-4ad5-aa19-ae713d837408

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
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
OFC Catheter Introducer Kit

GMDN Terms

Code Name
46455 Torque manipulation device

Identifiers

Type ID
Secondary M204502001AA0
Primary 00813132020446
Package 20813132020440

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 7.5 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep Dry