FDA UDI In Commercial Distribution 🇺🇸 United States

MicroAire®

DI: 00847399004635 · Model: 7100-011 · Microaire Surgical Instruments LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MicroAire®
Primary DI
00847399004635
Version / Model
7100-011
Company Name
Microaire Surgical Instruments LLC
Labeler DUNS
103056420
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-17
Public Version
1
Public Version Date
2022-09-26
Public Version Status
New
Public Device Record Key
7e2b5d38-0b4e-4e7e-89c8-f1c916885b7a

Device Description

REAMER COUPLER, HARRIS/AESCULAP®

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
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
KIJ Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment

GMDN Terms

Code Name
58189 Bone/joint surgical power tool motorized handpiece/set, pneumatic

Identifiers

Type ID
Primary 00847399004635