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Flex-Neck®

FDA UDI

Class II (US FDA UDI)

by Merit Medical Systems, Inc.

Identity

Trade Name
Flex-Neck® FDA UDI
Generic Name
Anaesthesia conduction catheter holder, sterile FDA UDI
Model / Reference
00884450330074 FDA UDI

Identifiers

Catalog Number
CF-4235/C FDA UDI
Primary DI / UDI-DI
00884450330074 FDA UDI
FDA Product Code
FJS FDA UDI
GMDN Term
Anaesthesia conduction catheter holder, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5630 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

No

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

Flex-Neck is a unique, combination product designed to securely insert an anaesthesia conduction catheter at the skin insertion site. With its locking mechanism and adhesive-backed pad, this device helps prevent catheter migration, making it an essential tool for surgeons and medical professionals.

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 18049ee3-ac48-4059-a6a2-c3b25a8c9714 34 fields · synced Jul 18, 2026