FDA UDI In Commercial Distribution 🇺🇸 United States

Beaver® Xstar®

DI: 30886158000229 · Model: 370568 · Beaver-Visitec International, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Beaver® Xstar®
Primary DI
30886158000229
Version / Model
370568
Catalog Number
370568
Company Name
Beaver-Visitec International, Inc.
Labeler DUNS
001406024
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-06
Public Version
1
Public Version Date
2024-06-14
Public Version Status
New
Public Device Record Key
62ccc117-4e7d-46dc-8d86-3e072a4bc34b

Device Description

BLADE MULTI SIDED SHARP ALL AROUND (100/SP)

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GES BLADE, SCALPEL

GMDN Terms

Code Name
37445 Manual scalpel blade, single-use

Identifiers

Type ID
Primary 30886158000229

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a dry place.