FDA.reportPublic FDA data

TubeClear

Primary DI
00850458007096
Brand
TubeClear
Company
ACTUATED MEDICAL, INC.
Model
G-1009
Device description
Clearing Stem
Published
2017-10-02
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Product Codes#

Code, Name table
CodeName
FPDTube, Feeding
KNTTubes, Gastrointestinal (And Accessories)

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FPDTube, FeedingGastroenterology, Urology2
KNTTubes, Gastrointestinal (And Accessories)Gastroenterology, Urology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K131052000
K172556000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K131052000TUBECLEAR MODEL 101 (WITH NEW CLEARING STEM NE AND G MODELS)Actuated Medical, Inc.2013-08-16KNT
K172556000TubeClear SystemActuated Medical, Inc.2018-06-29KNT

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10850458007093PackageGS15
20850458007090PackageGS110
00850458007096PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1085045800709310850458007093
2085045800709020850458007090
00850458007096008504580070968504580070960850458007096

GMDN Terms#

Term, Definition table
TermDefinition
Enteral feeding/decompression tube clearing stemA non-sterile, sheath-covered device intended to be used to mechanically clear a clog in an in situ nasogastric, nasoenteral, gastrostomy and/or jejunostomy tube, used for feeding and/or decompression, to maintain luminal patency. It consists of a sheath and a stem clog disrupter (e.g., a wire or rod) designed to be magnetically coupled with a motorized actuator which facilitates the forward and backward movement of the disrupter inside the sheath. It typically has a collar to restrict the inserted length, and a diameter, appropriate for the installed feeding/decompression tube. This is a single-use device.

Regulatory Flags#

DUNS number
791379030
Device count
1
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00850458007089TubeClearG-10082017-10-02
00850458007102TubeClearG-10102017-10-02
00850458007119TubeClearG-10112017-10-02
00850458007126TubeClearG-10122016-10-27
00850458007140TubeClearG-10142016-10-27
00850458007423TubeClear NE-10422016-10-27
00850458007430TubeClearNE-10432016-10-27
00850458007454TubeClearNE-10452017-10-02
00850458007485TubeClearNE-10482016-10-27
00850458007508TubeClearNE-10502016-10-27
00850458007553TubeClearNE-10552016-10-27
00850458007607TubeClearTC-06082017-03-02
00850458007614TubeClearTC-08122017-03-02
00850458007621TubeClearTC-10182017-10-02
00850458007010TubeClearControl Box Model 101101-US2016-09-08
00850458007362TubeClearNE-10362016-10-27
00850458007195GripTract-GI Endoscopic Tissue ManipulatorGT-GS1002025-12-23
00850458007041GripTract-GI Endoscopic Tissue ManipulatorGT-1012025-01-16
00850458007003TubeClearGJ-1422GJ-14222021-01-01
00850458007157GripTract-GI Endoscopic Tissue ManipulatorGT-CM1302025-01-16

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