← Back to catalogue

IV Administration Set, Non-Toxic, 10 mL

FDA UDI

Class II (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
IV Administration Set, Non-Toxic, 10 mL FDA UDI
Generic Name
Basic intravenous administration set, noninvasive FDA UDI
Device Name
Sterile-EO FDA UDI
Model / Reference
7029 FDA UDI
Description
Sterile-EO FDA UDI

Identifiers

Primary DI / UDI-DI
00840117327634 FDA UDI
FDA Product Code
FPA FDA UDI
LHI 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Basic intravenous administration set, noninvasive

IV Administration Set, Non-Toxic, 10 mL by Dynarex Corp. — 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

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

Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 24c89da1-dfe3-4465-9705-b970bd482801 33 fields · synced May 31, 2026