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Oasis

FDA UDI

Class II (US FDA UDI)

by American Health Service Sales Corporation

Identity

Trade Name
Oasis FDA UDI
Generic Name
Basic intravenous administration set, noninvasive FDA UDI
Device Name
Sterile IV Administration Set 15Dr/ml 100" With Injection Site. FDA UDI
Model / Reference
IV15 FDA UDI
Description
Sterile IV Administration Set 15Dr/ml 100" With Injection Site. FDA UDI

Identifiers

Primary DI / UDI-DI
B031IV150 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Basic intravenous administration set, noninvasive FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Basic intravenous administration set, noninvasive

Oasis by American Health Service Sales Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic intravenous administration set, noninvasive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
American Health Service Sales Corporation

Sources (1)

  • FDA UDI 5dd0c7f5-5859-4d5f-bf5f-01647843e79c 33 fields · synced Jun 8, 2026