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Nunc™ Universal™ Tube, 1.8mL externally-threaded, Non-2D

FDA UDI

Class I (US FDA UDI)

by Nalge Nunc International Corporation

Identity

Trade Name
Nunc™ Universal™ Tube, 1.8mL externally-threaded, Non-2D FDA UDI
Generic Name
General specimen container IVD, no additive/medium FDA UDI
Device Name
1.8ML EXTERNAL UNCODED WP BULK FDA UDI
Model / Reference
374503 FDA UDI
Description
1.8ML EXTERNAL UNCODED WP BULK FDA UDI

Identifiers

Primary DI / UDI-DI
10850016058543 FDA UDI
FDA Product Code
FMH FDA UDI
GMDN Term
General specimen container IVD, no additive/medium FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Nunc™ Universal™ Tube, 1.8mL externally-threaded, Non-2D by Nalge Nunc International Corporation — Class I — FDA UDI — listed in FDA GUDID

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nalge Nunc International Corporation

Sources (1)

  • FDA UDI 718f26d9-a571-469d-8200-1a3142cdea79 34 fields · synced Jun 9, 2026