FDA UDI In Commercial Distribution 🇺🇸 United States

SCANLAN® Ultimate® A/V Punch

DI: 00846159000191 · Model: 1001-626 · SCANLAN INTERNATIONAL INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SCANLAN® Ultimate® A/V Punch
Primary DI
00846159000191
Version / Model
1001-626
Catalog Number
1001-626
Company Name
SCANLAN INTERNATIONAL INC
Labeler DUNS
023055619
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-07
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
e49359dc-7de3-4ea0-87d4-76fb76232045

Device Description

SCANLAN® Ultimate® A/V Punch, 5.0 mm

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
Yes
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
KDC Instrument, Surgical, Disposable

GMDN Terms

Code Name
47914 Aorta punch, single-use

Identifiers

Type ID
Primary 00846159000191

Customer Contacts

Phone
651-298-0997