FDA UDI In Commercial Distribution 🇺🇸 United States

Bioseal Inc.

DI: 00630094183022 · Model: 18302/10 · BIOSEAL
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Bioseal Inc.
Primary DI
00630094183022
Version / Model
18302/10
Company Name
BIOSEAL
Labeler DUNS
186968939
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-05
Public Version
1
Public Version Date
2023-10-13
Public Version Status
New
Public Device Record Key
c7b1b66e-d471-4252-8c1a-da69e0e78f68

Device Description

Neonatal Stethoscope

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
LDE STETHOSCOPE, MANUAL

GMDN Terms

Code Name
13755 Mechanical stethoscope

Identifiers

Type ID
Package 10630094183029
Primary 00630094183022