BASEN

Primary DI
16978331170239
Brand
BASEN
Company
Dongguan Yiyingmei Technology Co., Ltd.
Model
BC-023
Device description
The Nasal Aspirator is intended for intermittent removal of nasal secretions and mucus from children (age 2-12 years old). This device is used in a home environment.
Published
2025-03-31
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
true
Sterile
false
Single use
false

Product Codes#

Code, Name table
CodeName
BTAPump, Portable, Aspiration (Manual Or Powered)

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
BTAPump, Portable, Aspiration (Manual Or Powered)General, Plastic Surgery2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K242028000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K242028000Nasal Aspirator (BC-021, BC-022, BC-023, BC-024, BC-025, BC-026)Dongguanshi Yiyingmei Technology Co., Ltd.2024-11-19BTA

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
16978331170239PackageGS160In Commercial Distribution
06978331170232PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
1697833117023916978331170239
06978331170232069783311702326978331170232

GMDN Terms#

Term, Definition table
TermDefinition
Nasal aspirator, electricA portable, hand-held, battery-powered suction device designed to enable an adult to gently suction and clear excessive mucus from the nasal passages of an infant or child to facilitate easier breathing. It consists of a handgrip that contains the batteries, a small electric pump that creates the suction, and typically has a silicone nozzle attached to a detachable, washable, collection cup at the distal end. It is designed for domestic use and is typically applied superficially the nasal opening (i.e., not inserted into the nasal cavity). This is a reusable device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
844241676
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
Serial number
true
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
06978331178016BASENYM-8012025-04-29
06978331178030BASENYM-8032025-04-29
06978331178054BASENYM-8052025-04-29
06978331178061BASENYM-8062025-04-29
06978331178085BASENYM-8082025-04-29
06978331170218BASENBC-0212025-03-31
06978331170232BASENBC-0232025-03-31
06978331170249BASENBC-0242025-03-31
06978331170256BASENBC-0252025-03-31
06978331170263BASENBC-0262025-03-31
06978331170270BASENBC-0222025-03-31
16978331170215BASENBC-0212025-03-31
16978331170246BASENBC-0242025-03-31
16978331170253BASENBC-0252025-03-31
16978331170260BASENBC-0262025-03-31
16978331170277BASENBC-0222025-03-31

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00860014862700GROWNSYOak Tech LLCBTA2026-01-10
00860014862717GROWNSYOak Tech LLCBTA2026-01-10
00860014862724GROWNSYOak Tech LLCBTA2026-01-10
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00810149098178R&D Batteries, Inc.R & D Batteries, Inc.BTA2025-10-27
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00860014577529GROWNSYOak Tech LLCBTA2025-08-26
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