FDA UDI In Commercial Distribution 🇺🇸 United States

Endeavour MD

DI: 00615375013441 · Model: 910176-13 · METREX RESEARCH, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Endeavour MD
Primary DI
00615375013441
Version / Model
910176-13
Company Name
METREX RESEARCH, LLC
Labeler DUNS
145963778
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-11-13
Public Version
1
Public Version Date
2023-11-21
Public Version Status
New
Public Device Record Key
d3c2864b-4d2f-4ff6-8f0d-038c3bbf924a

Device Description

FINAL ASSEMBLY, ENDEAVOUR™ MD, DOUBLE, INTERNATIONAL, JAW

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
No

Product Codes

Code Name
FSP Loupe, Diagnostic/Surgical

GMDN Terms

Code Name
32692 Surgical binoculars, reusable

Identifiers

Type ID
Primary 00615375013441

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store at Temperature of -4F to 104F (-20C to +40C); Relative Humidity of 10% to 85%; Atmospheric Pressure of 0.5 atm to 1.0 atm (500 hPa to 1060 hPa)