FDA UDI In Commercial Distribution 🇺🇸 United States

Beaver®

DI: 30886158001080 · Model: 375930 · Beaver-Visitec International, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Beaver®
Primary DI
30886158001080
Version / Model
375930
Catalog Number
375930
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
9c486f8e-cf4f-4785-a619-5d4f6330f20a

Device Description

BLADE 7.0MM CUTTING W S/SU (3/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
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
GES BLADE, SCALPEL

GMDN Terms

Code Name
46741 Ophthalmic knife, single-use

Identifiers

Type ID
Primary 30886158001080

Customer Contacts

Storage Conditions

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