FDA UDI In Commercial Distribution 🇺🇸 United States

Bioseal Inc.

DI: 00630094068121 · Model: 6812/100 · BIOSEAL
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Bioseal Inc.
Primary DI
00630094068121
Version / Model
6812/100
Company Name
BIOSEAL
Labeler DUNS
186968939
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-29
Public Version
1
Public Version Date
2024-02-06
Public Version Status
New
Public Device Record Key
2f15c578-adbd-4a3c-a80a-8cae0061769b

Device Description

Umbilical Tape

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
FOD DEVICE, OCCLUSION, UMBILICAL

GMDN Terms

Code Name
13983 Umbilical cord tape

Identifiers

Type ID
Package 10630094068128
Primary 00630094068121