AccessGUDID - DEVICE: Clinton Industries (00810045930763)

GUDID

Device Identifier (DI) Information

Brand Name: Clinton Industries
Version or Model: 6351
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 6351
Company Name: CLINTON INDUSTRIES, INC.

Primary DI Number: 00810045930763
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 021443502 *Terms of Use

Device Description: Power Series, Extra-Wide, Blood Drawing Chair with Padded Arms

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:	No
Prescription Use (Rx):	No
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?
10789	Blood donor chair/couch	A mains electricity (AC-powered) device used to position the patient in such a manner that a technician/nurse has easy access to the patient's arm for drawing blood. The armboard, that is attached to the chair, typically has lateral and height adjustments so that the patient's arm can be positioned in a location that is easily accessible to whoever is drawing the blood sample. This chair is electrically motorized and can be adjusted so that the donor can lie in a reclining position.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
INN	Chair, Adjustable, Mechanical

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: 1e923e17-a70b-4db6-b720-9e81c5195a53
Public Version Date: February 18, 2020
Public Version Number: 1
DI Record Publish Date: February 10, 2020

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: 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: No
Serial Number: Yes
Expiration Date: No
Manufacturing Date: Yes
Donation Identification Number: No CLOSE

Customer Contact

[?]

No Customer Contact currently defined

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