FDA UDI In Commercial Distribution 🇺🇸 United States

ENDO-SCRUB®

DI: 20681490465414 · Model: 1912023 · MEDTRONIC XOMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
ENDO-SCRUB®
Primary DI
20681490465414
Version / Model
1912023
Company Name
MEDTRONIC XOMED, INC.
Labeler DUNS
835465063
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2016-04-30
Public Version
7
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
5b9c9447-0712-4325-9068-3a162c9aa3eb

Device Description

SHEATH 1912023 5PK 2.7MM/0DEG XOMED

Device Characteristics

Single Use
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
EOB NASOPHARYNGOSCOPE (FLEXIBLE OR RIGID)

GMDN Terms

Code Name
44711 Optical medical device procedural cover

Identifiers

Type ID
Primary 20681490465414
Unit of Use 00681490465410

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K982594 000

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 2.7 Millimeter
Angle 0.0 degree