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Mtp

FDA UDI

Class II (US FDA UDI)

by Medical Technology Products Inc

Identity

Trade Name
MTP FDA UDI
Generic Name
Non-absorbing intravenous administration set FDA UDI
Device Name
NITRO ADMIN SET FDA UDI
Model / Reference
1260 FDA UDI
Description
NITRO ADMIN SET FDA UDI

Identifiers

Catalog Number
SO1260 FDA UDI
Primary DI / UDI-DI
28500042541265 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Non-absorbing intravenous administration set 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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Non-absorbing intravenous administration set

Mtp by Medical Technology Products Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-absorbing intravenous administration set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medical Technology Products Inc

Sources (1)

  • FDA UDI 371a249d-f3a9-4ec3-abcb-541f4b7b7c4a 35 fields · synced May 30, 2026