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Namic

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
NAMIC FDA UDI
Generic Name
Stopcock FDA UDI
Device Name
MTO PML 36 PEDIATRIC FLL-MLL - OEM FDA UDI
Model / Reference
80621362 FDA UDI
Description
MTO PML 36 PEDIATRIC FLL-MLL - OEM FDA UDI

Identifiers

Catalog Number
80621362 FDA UDI
Primary DI / UDI-DI
40193489067348 FDA UDI
FDA Product Code
DRI FDA UDI
GMDN Term
Stopcock FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.2620 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

Yes

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 I — 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

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Manufacturer

Sources (1)

  • FDA UDI 595c7771-86b7-49b3-b21d-7429a6b64d4a 36 fields · synced May 30, 2026