AccessGUDID - DEVICE: BioSkin (00850017044920)

GUDID

Device Identifier (DI) Information

Brand Name: BioSkin
Version or Model: 2016BKMLM
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: LIBERTY GLOVE & SAFETY, LLC

Primary DI Number: 00850017044920
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 111313244 *Terms of Use

Device Description: Black PF nitrile glove, 100pcs/bx

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):	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?
58286	Thermal vapour lung treatment system catheter	A sterile flexible tube with an inflatable balloon at the distal end designed to deliver heated sterile water vapour into a lung affected by emphysema to achieve bronchoscopic lung volume reduction through the application of high thermal vapour energy to the lung segment targeted for treatment. The catheter is introduced via the working channel of a bronchoscope, the occlusion balloon is inflated in the airway, and thermal water vapour is released to produce a limited energy transfer which is restricted to the airways and diseased parenchyma in the targeted lung segment. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LZA	Polymer Patient Examination Glove

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: 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: 046d6a10-cc9c-438f-a215-ee0ae52d3547
Public Version Date: August 30, 2024
Public Version Number: 1
DI Record Publish Date: August 22, 2024

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

Customer Contact

[?]

No Customer Contact currently defined

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