FDA UDI In Commercial Distribution 🇺🇸 United States

Brasseler USA

DI: 00887919632993 · Model: 5018364U0 · Peter Brasseler Holdings, LLC
Product Codes
0
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Brasseler USA
Primary DI
00887919632993
Version / Model
5018364U0
Company Name
Peter Brasseler Holdings, LLC
Labeler DUNS
082080136
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-12
Public Version
3
Public Version Date
2023-02-24
Public Version Status
Update
Public Device Record Key
c7d63c98-5b7e-4879-ba40-afc35b704872

Device Description

K0189 LARGE GROUP SEQ STARTER

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

GMDN Terms

Code Name
40529 Rotary/reciprocating endodontic file/rasp, reusable

Identifiers

Type ID
Primary 00887919632993