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Nova

FDA UDI

Class I (US FDA UDI)

by Nova Biomedical Corporation

Identity

Trade Name
Nova FDA UDI
Generic Name
Surgical traction tensioner connector FDA UDI
Device Name
Nova Biomedical® Capillary Tube Clot Catcher FDA UDI
Model / Reference
Nova FDA UDI
Description
Nova Biomedical® Capillary Tube Clot Catcher FDA UDI

Identifiers

Catalog Number
38846 FDA UDI
Primary DI / UDI-DI
00385480388467 FDA UDI
FDA Product Code
LXG FDA UDI
GMDN Term
Surgical traction tensioner connector FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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

No

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

Category: Surgical traction tensioner connector

Nova by Nova Biomedical Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical traction tensioner connector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 306327c0-387d-408b-956c-518062f03c2b 35 fields · synced Jun 8, 2026