FDA UDI In Commercial Distribution 🇺🇸 United States

Merocel

DI: 30886158011973 · Model: 223622 · Beaver-Visitec International, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
Merocel
Primary DI
30886158011973
Version / Model
223622
Company Name
Beaver-Visitec International, Inc.
Labeler DUNS
001406024
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2016-09-19
Public Version
4
Public Version Date
2023-10-03
Public Version Status
Update
Public Device Record Key
01e2e44b-9012-4c32-8e22-a37a1bf4e068

Device Description

Wipe with Wick and Corneal Shield

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
Yes
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
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
HOZ Sponge, ophthalmic

GMDN Terms

Code Name
13704 Ophthalmic sponge

Identifiers

Type ID
Primary 30886158011973
Unit of Use 00886158011972

Customer Contacts

Storage Conditions

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