← Back to catalogue

Namic

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
NAMIC FDA UDI
Generic Name
Stopcock FDA UDI
Device Name
MTO SC 3W HP RA ON NB BARD AUSTRALIA FDA UDI
Model / Reference
80601005 FDA UDI
Description
MTO SC 3W HP RA ON NB BARD AUSTRALIA FDA UDI

Identifiers

Catalog Number
80601005 FDA UDI
Primary DI / UDI-DI
20193489067160 FDA UDI
FDA Product Code
DTL FDA UDI
GMDN Term
Stopcock FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4290 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Stopcock

Namic by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stopcock.

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

Sources (1)

  • FDA UDI 760aad97-b351-4f02-9082-f16404287d6b 36 fields · synced May 30, 2026