FDA UDI In Commercial Distribution 🇺🇸 United States

MICROCUFF™

DI: 10889483565162 · Model: 35210 · SUNMED, LLC
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
MICROCUFF™
Primary DI
10889483565162
Version / Model
35210
Catalog Number
35210
Company Name
SUNMED, LLC
Labeler DUNS
069009268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-12
Public Version
1
Public Version Date
2026-01-20
Public Version Status
New
Public Device Record Key
1e68b7bd-d12a-44b8-9983-ca41d2ad13ad

Device Description

MICROCUFF™ ENDOTRACHEAL TUBE FOR ADULTS/Oral/Nasal Magill, Murphy Eye/Radiopaque

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
BTR Tube, Tracheal (W/Wo Connector)

GMDN Terms

Code Name
46967 Basic endotracheal tube, single-use

Identifiers

Type ID
Package 20889483565169
Primary 10889483565162
Package 30889483565166
Previous 00609038352107

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 6.9 Millimeter