AccessGUDID - DEVICE: Closed Wound Suction (00801741050169)

GUDID

Device Identifier (DI) Information

Brand Name: Closed Wound Suction
Version or Model: 0085320
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 0085320
Company Name: C. R. Bard, Inc.

Primary DI Number: 00801741050169
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 016898496 *Terms of Use

Device Description: ReliaVac 100 Closed Wound Suction Kit, Medium Suction, 100cc Evacuator, Y-Connecting Tube, Silicone Round Drain, Medium-Large 3/16", (4.7mm) O.D., 10"(25.4cm) Hole Pattern, X-Ray Opaque Stripe, Attached Trocar

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?
35824	Closed-wound drainage kit	A collection of devices designed to remove fluids or purulent material from a closed-wound in a controlled manner. It includes a container (the receptacle or reservoir), drains/catheters, connectors, a grasping device and possibly a trocar for placing the drains/catheters into the site. The reservoir will usually be provided with graduated markers along its side to facilitate the approximate measurement of the collected fluids. This is a single-use device.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
GCY	APPARATUS, SUCTION, SINGLE PATIENT USE, PORTABLE, NONPOWERED

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
Outer Diameter: 4.7 Millimeter

Device Record Status

Public Device Record Key: d9c09544-47a3-4ef5-bf77-c008f14bd078
Public Version Date: February 05, 2021
Public Version Number: 2
DI Record Publish Date: September 22, 2020