FDA UDI In Commercial Distribution 🇺🇸 United States

Triton®

DI: 00613994421791 · Model: 703002-R · MEDTRONIC POWERED SURGICAL SOLUTIONS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Triton®
Primary DI
00613994421791
Version / Model
703002-R
Company Name
MEDTRONIC POWERED SURGICAL SOLUTIONS
Labeler DUNS
098308849
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-29
Public Version
5
Public Version Date
2023-11-17
Public Version Status
Update
Public Device Record Key
540d6110-f509-4fa0-9b8a-66f0d5dc01f9

Device Description

ACCY 703002-R TRITON PNEUMATIC CO REFURB

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KFK SAW, PNEUMATICALLY POWERED

GMDN Terms

Code Name
41267 Surgical power tool system control unit, pneumatic

Identifiers

Type ID
Primary 00613994421791

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K870157 000