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Merit Advance®

FDA UDI

Class II (US FDA UDI)

by Merit Medical Systems, Inc.

Identity

Trade Name
Merit Advance® FDA UDI
Generic Name
Anaesthesia conduction catheter holder, sterile FDA UDI
Model / Reference
00884450015698 FDA UDI

Identifiers

Primary DI / UDI-DI
00884450015698 FDA UDI
FDA Product Code
DRC FDA UDI
GMDN Term
Anaesthesia conduction catheter holder, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1390 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Anaesthesia conduction catheter holder, sterile

The Merit Advance device is a sterile, single-use anaesthesia conduction catheter holder used to secure an anaesthesia conduction catheter at the skin insertion site. It features a locking mechanism that prevents catheter migration and is designed for implantable use in cardiovascular regulation.

Similar devices

Also classified as Anaesthesia conduction catheter holder, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Merit Medical Systems, Inc.

Sources (1)

  • FDA UDI 3d656c1e-2c8e-4dd5-932d-ffc4fc3fbbbd 33 fields · synced Jul 10, 2026