AccessGUDID - DEVICE: Perifix® (04046964178962)

GUDID

Device Identifier (DI) Information

Brand Name: Perifix®
Version or Model: 332283
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 332283
Company Name: B. BRAUN MEDICAL INC.

Primary DI Number: 04046964178962
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 50
Labeler D-U-N-S® Number*: 002397347 *Terms of Use

Device Description: PERIFIX® Catheter Connector - use with PERIFIX® 20 Ga. to 24 Ga.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	Yes
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
64468	NRFit/non-ISO80369-standardized linear connector	A small, non-powered, noninvasive, tubular, two-way/linear connector with an NRFit connection (designed according to ISO 80369-6 for neuraxial applications) at one end and a connection which is not designed according to ISO 80369 at the other end (typically barbed, conical, threaded or non-Luer-slip), intended to connect a neuraxial device (e.g., epidural catheter, syringe) with an NRFit connection typically with tubing. It does not have a Luer connection(s), and does not incorporate a filter, valve, clamp nor tubing. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
CAZ	Anesthesia conduction kit
BSO	CATHETER, CONDUCTION, ANESTHETIC

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 750abbe0-826d-4738-982e-38861998016d
Public Version Date: November 12, 2020
Public Version Number: 6
DI Record Publish Date: September 23, 2016

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: 04046964178955 CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: No
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: Yes
Serial Number: No
Expiration Date: Yes
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1(800)227-2862
Email: BBMUS_Service.EmailOrders@bbraun.com

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