Perifix Catheter Connector
by B. Braun Medical, Inc. 3 variants
510(k) K022019
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK022019 | Date1 Aug 2002 | StatusActive |
Recalls
No FDA recalls found in the data synced 8 Nov 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- BSO
- FDA applicant
- B.Braun Medical, Inc.
- Device class
- Class II
- Regulation
- 21 CFR Part 868.5120
- Advisory committee
- Anesthesiology
- FDA decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 26 Sep 2026
A catheter connector for regional anaesthesia, designed for use with epidural and peripheral nerve block catheters. It features a transparent lid for clear visibility of the catheter and a color-coded body to distinguish between two different sizes.
Supplied as a non-sterile, reusable device intended for use in clinical settings. It is compatible with Perifix 19 Ga catheters and is authorised under FDA 510(k) clearance K022019, classified as a Class II device under regulation number 868.5120 with product code BSO.
From the manufacturer
Perifix® Catheter Connectors -. Selection of catheter connectors. Work with all B. Braun Epidural and PNB catheters.
PERIFIX ® Catheter Connector - use with PERIFIX ® 19 Ga.