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Bioseal

FDA UDI

Class II (US FDA UDI)

by Bioseal

Identity

Trade Name
Bioseal FDA UDI
Generic Name
Nasogastric feeding tube FDA UDI
Device Name
Levin Tube Radiopaque 18FR FDA UDI
Model / Reference
19718/12 FDA UDI
Description
Levin Tube Radiopaque 18FR FDA UDI

Identifiers

Primary DI / UDI-DI
00630094197180 FDA UDI
FDA Product Code
GAZ FDA UDI
GMDN Term
Nasogastric feeding tube 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nasogastric feeding tube

Bioseal by Bioseal — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasogastric feeding tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bioseal

Sources (1)

  • FDA UDI 26baf5d5-d6bd-4dd3-93a5-bc80f553f00c 33 fields · synced May 30, 2026