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Momcozy

FDA UDI

Class II (US FDA UDI)

by Shenzhen Lutejiacheng Technology Co., Ltd.

Identity

Trade Name
Momcozy FDA UDI
Generic Name
Nasal aspirator, electric FDA UDI
Model / Reference
NS13 FDA UDI

Identifiers

Primary DI / UDI-DI
06975740361558 FDA UDI
FDA Product Code
BTA FDA UDI
GMDN Term
Nasal aspirator, electric FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4780 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Nasal aspirator, electric

Momcozy by Shenzhen Lutejiacheng Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal aspirator, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f2bd8aa8-a767-462a-9031-3b17cf19c745 32 fields · synced Jun 1, 2026