FDA UDI In Commercial Distribution 🇺🇸 United States

Needle

DI: 08800019101789 · Model: BMN2423 · B& L Biotech, inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Needle
Primary DI
08800019101789
Version / Model
BMN2423
Company Name
B& L Biotech, inc.
Labeler DUNS
687338285
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-15
Public Version
1
Public Version Date
2020-06-23
Public Version Status
New
Public Device Record Key
55b37c05-9c8a-4897-9ecc-6e3364fe30dd

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
No
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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
EKR Plugger, Root Canal, Endodontic

GMDN Terms

Code Name
45247 Endodontic obturation system

Identifiers

Type ID
Primary 08800019101789