FDA UDI In Commercial Distribution 🇺🇸 United States

Brasseler USA

DI: 00887919480754 · Model: 5007214M0 · Peter Brasseler Holdings, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Brasseler USA
Primary DI
00887919480754
Version / Model
5007214M0
Company Name
Peter Brasseler Holdings, LLC
Labeler DUNS
082080136
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-01
Public Version
1
Public Version Date
2022-12-09
Public Version Status
New
Public Device Record Key
479fc355-96ca-4d2e-9499-0f57230f9b4a

Device Description

13-S01185 8.0MM ROUND CEBATOME

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
GFF BUR, SURGICAL, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
45553 Orthopaedic bur, single-use

Identifiers

Type ID
Primary 00887919480754