FDA UDI In Commercial Distribution 🇺🇸 United States

ENDO-SCRUB®

DI: 00763000008147 · Model: 1852000 · MEDTRONIC XOMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDO-SCRUB®
Primary DI
00763000008147
Version / Model
1852000
Company Name
MEDTRONIC XOMED, INC.
Labeler DUNS
835465063
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-31
Public Version
2
Public Version Date
2018-07-06
Public Version Status
New
Public Device Record Key
4aef31c8-421c-47fb-acd6-7b6fdd092047

Device Description

FOOTSWITCH 1852000 ENDO-SCRUB 2 ROHS

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EOB Nasopharyngoscope (flexible or rigid)

GMDN Terms

Code Name
36336 Foot-switch, electrical

Identifiers

Type ID
Primary 00763000008147

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K902683 000