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Meconium Aspirator Tinted

FDA UDI

Class I (US FDA UDI)

by Neotech Products LLC

Identity

Trade Name
Meconium Aspirator Tinted FDA UDI
Generic Name
Airway suction catheter FDA UDI
Model / Reference
812594010811 FDA UDI

Identifiers

Catalog Number
NO102B FDA UDI
Primary DI / UDI-DI
00812594010811 FDA UDI
FDA Product Code
BSY FDA UDI
GMDN Term
Airway suction catheter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6810 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Airway suction catheter

Meconium Aspirator Tinted by Neotech Products LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Airway suction catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neotech Products LLC

Sources (1)

  • FDA UDI 18620b18-7743-4f9a-80b0-cd36bcdf287c 33 fields · synced Jun 1, 2026