FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10888551004190 · Model: MID7BA10DL-MN · STERILMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10888551004190
Version / Model
MID7BA10DL-MN
Catalog Number
7BA10DL-MN
Company Name
STERILMED, INC.
Labeler DUNS
175899459
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-06-18
Public Version
2
Public Version Date
2019-08-14
Public Version Status
Update
Public Device Record Key
ab542780-7b04-4ac4-99d8-28e2e058a5ce

Device Description

BUR DIAMOND LEGEND SYSTEM

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
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
Ethylene Oxide

Product Codes

Code Name
GFF BUR, SURGICAL, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
45553 Orthopaedic bur, single-use

Identifiers

Type ID
Primary 10888551004190

Customer Contacts