AccessGUDID - DEVICE: ClipVac (10885403459870)

GUDID

Device Identifier (DI) Information

Brand Name: ClipVac
Version or Model: 5575
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 5575
Company Name: CAREFUSION 2200, INC

Primary DI Number: 10885403459870
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 832696038 *Terms of Use

Device Description: ClipVac Disposable Filter Assembly - BD Surgical Clipper

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":	No
For Single-Use:	Yes
Prescription Use (Rx):	No
Over the Counter (OTC):	Yes
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?
62749	Surgical hair clippers suction system tubing set	A non-sterile length of flexible tubing and associated items intended to be used with surgical hair clippers as a component of a surgical hair clippers suction system, during removal/collection of cut hair through suction, typically as part of hair removal prior to surgery. The tubing is made of synthetic polymer material(s) and typically includes an open tip/nozzle at one end, intended to be attached to the clippers, and a hair collection container with filter at the other end, intended to be attached to the system suction pump. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GEY	MOTOR, SURGICAL INSTRUMENT, AC-POWERED

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: No
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: 1f5b46bc-e703-4831-aa48-484e7ad3c29f
Public Version Date: April 02, 2019
Public Version Number: 1
DI Record Publish Date: March 25, 2019

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
50885403459878	40	10885403459870		In Commercial Distribution	Box

Secondary DI

[?]

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

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found 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: No
Manufacturing Date: Yes
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1(800)523-0502
Email: Customer_Support@BD.com

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