AccessGUDID - DEVICE: EndoRotor® Purge Kit (Single) (00854172008087)

GUDID

Device Identifier (DI) Information

Brand Name: EndoRotor® Purge Kit (Single)
Version or Model: ER 60-01
Commercial Distribution Status: In Commercial Distribution
Catalog Number: ER 60-01
Company Name: INTERSCOPE, INC

Primary DI Number: 00854172008087
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 968227913 *Terms of Use

Device Description: No description.

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):	Yes
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?
63527	Device lumen washing/disinfection attachment, single-use	A device intended to be fitted to a luminal device (e.g., catheter, endoscope air/water channel, vitrectomy handpiece) to assist with the washing and/or disinfection of the lumen of the device during a medical/surgical procedure and/or for maintenance pre/post procedure. It is typically in the form of a small, cylindrical rod(s) which may have a button/switch which controls the supply of air and/or water; it may also include tubing and/or be used in conjunction with a syringe, device washer/disinfector, and/or water tap. This is a single-use device.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
PTE	Endoscopic Morcellator Gastroenterology

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: 941eef5d-d43d-4a3d-b76d-a4039e42425b
Public Version Date: April 07, 2021
Public Version Number: 1
DI Record Publish Date: March 30, 2021

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

Customer Contact

[?]

Phone: 1-800-461-4289
Email: info@interscopemed.com

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