FDA UDI In Commercial Distribution 🇺🇸 United States

TubeClear

DI: 00850458007010 · Model: Control Box Model 101 · ACTUATED MEDICAL, INC.
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TubeClear
Primary DI
00850458007010
Version / Model
Control Box Model 101
Catalog Number
101-US
Company Name
ACTUATED MEDICAL, INC.
Labeler DUNS
791379030
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-08
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
9ebec681-32b5-494b-8e22-bda4086af1d2

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
Yes
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
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
Primary 00850458007010

Premarket Submissions

Submission Number Supplement Number
K131052 000