← Back to catalogue

Nautilus Delta

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name
NAUTILUS DELTA FDA UDI
Generic Name
Central venous catheter navigation system, electrocardiographic FDA UDI
Device Name
Refurbished Display FDA UDI
Model / Reference
9770322X FDA UDI
Description
Refurbished Display FDA UDI

Identifiers

Catalog Number
9770322X FDA UDI
Primary DI / UDI-DI
00801741137082 FDA UDI
FDA Product Code
LJS FDA UDI
GMDN Term
Central venous catheter navigation system, electrocardiographic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5970 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Central venous catheter navigation system, electrocardiographic

Nautilus Delta by Bard Access Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Central venous catheter navigation system, electrocardiographic.

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

Manufacturer
Bard Access Systems, Inc.

Sources (1)

  • FDA UDI f5de7fbd-0733-43b3-84b0-89c75c7729a9 36 fields · synced Jun 9, 2026