← Back to catalogue

Orion

FDA UDI

Class II (US FDA UDI)

by Nurse Assist, Inc.

Identity

Trade Name
ORION FDA UDI
Generic Name
Wound irrigation sterile saline FDA UDI
Device Name
100ML STERILE SALINE SCREW TOP FDA UDI
Model / Reference
30296 FDA UDI
Description
100ML STERILE SALINE SCREW TOP FDA UDI

Identifiers

Primary DI / UDI-DI
B150302964 FDA UDI
510(k) Number
K901079 FDA UDI
FDA Product Code
BTO FDA UDI
GMDN Term
Wound irrigation sterile saline FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5800 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wound irrigation sterile saline

Orion by Nurse Assist, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound irrigation sterile saline.

Cleared under the same submission

K901079 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Nurse Assist, Inc.

Sources (1)

  • FDA UDI dd7b3e06-0e84-4c93-87ae-b6971d82202a 34 fields · synced May 30, 2026