FDA UDI In Commercial Distribution 🇺🇸 United States

Bioseal Inc.

DI: 00630094176307 · Model: 17630/20 · BIOSEAL
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Bioseal Inc.
Primary DI
00630094176307
Version / Model
17630/20
Company Name
BIOSEAL
Labeler DUNS
186968939
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-28
Public Version
1
Public Version Date
2023-10-06
Public Version Status
New
Public Device Record Key
66200df3-3a89-4359-98d2-a70963e52fe5

Device Description

Vascular Wire 25g - 18"

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KDC INSTRUMENT, SURGICAL, DISPOSABLE

GMDN Terms

Code Name
14457 Wire ligature

Identifiers

Type ID
Package 10630094176304
Primary 00630094176307