← Back to catalogue

Celerity

FDA UDI

Class II (US FDA UDI)

by Navilyst Medical, Inc.

Identity

Trade Name
Celerity FDA UDI
Generic Name
Central venous catheter navigation system control unit FDA UDI
Device Name
Celerity 7.2V Li Ion Battery Accessory FDA UDI
Model / Reference
H787471460 FDA UDI
Description
Celerity 7.2V Li Ion Battery Accessory FDA UDI

Identifiers

Primary DI / UDI-DI
H787471460 FDA UDI
FDA Product Code
LJS FDA UDI
GMDN Term
Central venous catheter navigation system control unit 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 control unit

Celerity by Navilyst Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Central venous catheter navigation system control unit.

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
Navilyst Medical, Inc.

Sources (1)

  • FDA UDI 80e7f89d-e7a3-4aac-9b4c-edfaf6c5d0d1 34 fields · synced May 30, 2026