FDA UDI In Commercial Distribution 🇺🇸 United States

Aztec

DI: B87110221100 · Model: 10-22110 · Aztecmed/Ent LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Aztec
Primary DI
B87110221100
Version / Model
10-22110
Catalog Number
10-22110
Company Name
Aztecmed/Ent LLC
Labeler DUNS
117559084
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-15
Public Version
1
Public Version Date
2022-02-23
Public Version Status
New
Public Device Record Key
d7b75b21-9e8f-4350-ba37-89aaf36e2a12

Device Description

Quickert Grooved Director

Device Characteristics

Single Use
No
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
No
Has Manufacturing Date
No
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
MDM Instrument, Manual, Surgical, General Use

GMDN Terms

Code Name
35047 ENT elevator

Identifiers

Type ID
Primary B87110221100