FDA UDI In Commercial Distribution 🇺🇸 United States

EndoEar™ ENDOSCOPE, 3MM X 150MM, 30 DEG.

DI: 00844505012256 · Model: EE-0330 · Grace Medical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
EndoEar™ ENDOSCOPE, 3MM X 150MM, 30 DEG.
Primary DI
00844505012256
Version / Model
EE-0330
Company Name
Grace Medical, Inc.
Labeler DUNS
030849173
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-05
Public Version
2
Public Version Date
2025-12-15
Public Version Status
Update
Public Device Record Key
e19f595a-56a8-4909-b531-336f631e0b9e

Device Description

EndoEar™ ENDOSCOPE 3.0 MM x 150 MM 30°

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
No
Has Serial Number
Yes
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
Ethylene Oxide, Moist Heat or Steam Sterilization, Hydrogen Peroxide

Product Codes

Code Name
EOB Nasopharyngoscope (Flexible Or Rigid)

GMDN Terms

Code Name
44929 Otoscope, endoscopic

Identifiers

Type ID
Primary 00844505012256

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K981751 000