AccessGUDID - DEVICE: Perifix® (04046964180002)

GUDID

Device Identifier (DI) Information

Brand Name: Perifix®
Version or Model: 333539
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 333539
Company Name: B. BRAUN MEDICAL INC.

Primary DI Number: 04046964180002
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 25
Labeler D-U-N-S® Number*: 002397347 *Terms of Use

Device Description: 20 Ga. x 40 in. Polyamide/Polyurethane PERIFIX® ONE Pediatric Catheter - closed tip with catheter connector and threading assist guide

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:	Yes
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?
34842	Epidural anaesthesia set, non-medicated	A collection of devices intended for the administration of an analgesic or anaesthetic agent (not included) to the epidural space for the management of pain. It includes a needle and/or a catheter with additional procedural devices (e.g., syringe, dressings, guidewire, introducer), and may be intended for single- or continuous-administration. It is not intended for intrathecal anaesthesia This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
OGE	Epidural anesthesia kit

FDA Premarket Submission

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

Device Exempt from Premarket Submission: Yes 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
Device Size Text, specify: Gauge (Catheter) : 20

Device Record Status

Public Device Record Key: 732d1611-561e-46ae-92ef-c86867cfb873
Public Version Date: February 17, 2021
Public Version Number: 7
DI Record Publish Date: September 23, 2016