FDA UDI In Commercial Distribution 🇺🇸 United States

Bioseal Inc.

DI: 00630094046372 · Model: 4637/25 · BIOSEAL
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Bioseal Inc.
Primary DI
00630094046372
Version / Model
4637/25
Company Name
BIOSEAL
Labeler DUNS
186968939
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-23
Public Version
1
Public Version Date
2024-01-31
Public Version Status
New
Public Device Record Key
3c0cd543-9b75-45e9-b451-82c8f9507d83

Device Description

Muslin

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
NAB Gauze / sponge,nonresorbable for external use

GMDN Terms

Code Name
61949 Personal care kit

Identifiers

Type ID
Package 10630094046379
Primary 00630094046372