FDA UDI In Commercial Distribution 🇺🇸 United States

TubeClear

DI: 00850458007553 · Model: NE-1055 · ACTUATED MEDICAL, INC.
Product Codes
2
GMDN Terms
2
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
TubeClear
Primary DI
00850458007553
Version / Model
NE-1055
Company Name
ACTUATED MEDICAL, INC.
Labeler DUNS
791379030
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-27
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
1f4c7986-6a0e-4244-92b3-f86eef4bcf57

Device Description

Clearing Stem

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FPD Tube, Feeding
KNT Tubes, Gastrointestinal (And Accessories)

GMDN Terms

Code Name
58974 Enteral feeding/decompression tube clearing stem
58973 Enteral feeding/decompression tube clearing actuator

Identifiers

Type ID
Package 20850458007557
Primary 00850458007553
Package 10850458007550

Premarket Submissions

Submission Number Supplement Number
K131052 000