FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00650862260229 · Model: 26022 · Atrium Medical Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00650862260229
Version / Model
26022
Company Name
Atrium Medical Corporation
Labeler DUNS
051798999
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
3
Public Version Date
2020-10-15
Public Version Status
Update
Public Device Record Key
e178e903-1eab-4006-8175-fedeabd1ddff

Device Description

TUNNELER, 7MM BLUNT TIPS

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
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
DWS INSTRUMENTS, SURGICAL, CARDIOVASCULAR

GMDN Terms

Code Name
35950 Vascular graft tunneller

Identifiers

Type ID
Primary 00650862260229