FDA UDI In Commercial Distribution 🇺🇸 United States

Endocept

DI: 09335006007397 · Model: 1 · WHITELEY CORPORATION PTY LTD
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Endocept
Primary DI
09335006007397
Version / Model
1
Company Name
WHITELEY CORPORATION PTY LTD
Labeler DUNS
750968679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-12
Public Version
1
Public Version Date
2025-06-20
Public Version Status
New
Public Device Record Key
b7e045d1-0177-4213-a046-b16e96e19921

Device Description

Multi-function enzymatic detergent for manual and automated reprocessing of surgical instruments and flexibles endoscopes

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
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FLG Cleaner, Ultrasonic, Medical Instrument

GMDN Terms

Code Name
63385 Medical device cleaning agent

Identifiers

Type ID
Package 19335006007448
Primary 09335006007397

Customer Contacts

Phone
+61249619333