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Curved Sucker XL (N208-B)

FDA UDI

Class II (US FDA UDI)

by Neotech Products LLC

Identity

Trade Name
Curved Sucker XL (N208-B) FDA UDI
Generic Name
Airway suction catheter FDA UDI
Model / Reference
10812594012577 FDA UDI

Identifiers

Catalog Number
N208-B FDA UDI
Primary DI / UDI-DI
00812594012570 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Airway suction catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Curved Sucker XL (N208-B) by Neotech Products LLC — Class II — 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 c05ea2f3-3f8d-4905-8ae3-7a7603e488f1 33 fields · synced May 30, 2026