FDA UDI In Commercial Distribution 🇺🇸 United States

Ultracell®

DI: 30886158012086 · Model: S90900 · Beaver-Visitec International, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ultracell®
Primary DI
30886158012086
Version / Model
S90900
Catalog Number
S90900
Company Name
Beaver-Visitec International, Inc.
Labeler DUNS
001406024
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-27
Public Version
1
Public Version Date
2024-07-05
Public Version Status
New
Public Device Record Key
551c4fbc-f7ca-43ca-92dd-85ba639267c3

Device Description

'INSTRUMENT WIPE, FOIL POUCHED 3'' X 3'' X 2MM (300/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
Radiation Sterilization

Product Codes

Code Name
HOZ Sponge, ophthalmic

GMDN Terms

Code Name
61965 Medical device cleaning sponge/set

Identifiers

Type ID
Primary 30886158012086

Customer Contacts

Storage Conditions

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