AccessGUDID - DEVICE: Simpulse (00801741010354)

GUDID

Device Identifier (DI) Information

Brand Name: Simpulse
Version or Model: 0037690
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 0037690
Company Name: Davol Inc.

Primary DI Number: 00801741010354
Issuing Agency: GS1
Commercial Distribution End Date: December 28, 2028
Device Count: 1
Labeler D-U-N-S® Number*: 001191048 *Terms of Use

Device Description: Dual Spike Adapter

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?
66959	Surgical irrigation/aspiration Y-piece connector	A tubular device designed with two inlets and one outlet openings intended to enable appropriate connection between a surgical/aspiration system/pump (e.g., connects to the pump spike) and the tubing lines that connect to a dual irrigation bag configuration. It may also be referred to as a dual spike adaptor. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FQH	LAVAGE, JET

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: 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
No Device Sizes

Device Record Status

Public Device Record Key: 33cc462c-085a-4349-9129-58e1a238e260
Public Version Date: October 22, 2024
Public Version Number: 4
DI Record Publish Date: December 23, 2015

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
10801741010351	10	00801741010354	2028-12-28	In Commercial Distribution	CA

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: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1(800)562-0027
Email: medical.services@bd.com

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