FDA UDI In Commercial Distribution 🇺🇸 United States

Bioseal Inc.

DI: 00630094194110 · Model: 19411/24 · BIOSEAL
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Bioseal Inc.
Primary DI
00630094194110
Version / Model
19411/24
Company Name
BIOSEAL
Labeler DUNS
186968939
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-11
Public Version
1
Public Version Date
2023-10-19
Public Version Status
New
Public Device Record Key
6f8580ea-aa41-41ee-befb-3cff5c691099

Device Description

BIG O Sponge GREEN

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
EFQ GAUZE/SPONGE, INTERNAL

GMDN Terms

Code Name
44971 General-purpose surgical sponge

Identifiers

Type ID
Package 10630094194117
Primary 00630094194110