AccessGUDID - DEVICE: Natus® (00382830056182)

GUDID

Device Identifier (DI) Information

Brand Name: Natus®
Version or Model: NT999110
Commercial Distribution Status: In Commercial Distribution
Catalog Number: NT999110
Company Name: NATUS MEDICAL INCORPORATED

Primary DI Number: 00382830056182
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 081325959 *Terms of Use
Previous DI: 10381780034544

Device Description: BURR HOLE RESERVOIR AND SILICONE CAP WITH F8 SIDE ARM (Polypropylene - Ø 6.4 mm - Depth 2.5 mm)

Device Characteristics

What MRI safety information does the labeling contain?	MR Safe
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):	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?
61375	Cranial port/reservoir	A sterile, implantable chamber intended to be connected to an intracerebral catheter for infusion/injection of materials (e.g., chemotherapeutic agents, radioisotopes) into the brain (e.g., cerebral ventricles, cystic tumours, tumour cavities); it may also be used for drainage of cerebrospinal fluid (CSF) from the ventricles and as part of a ventriculo-peritoneal/atrial shunt system. The device is implanted subcutaneously and materials infused/injected with a needle via hypodermic puncture flow into the target site through the connected catheter. It is typically a bulb-shaped device made of plastic material (e.g., polypropylene, silicone). This is a single-use device.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
JXG	Shunt, Central Nervous System And Components

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K925810	000

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
Device Size Text, specify: Regular Reservoir 2.5mm Depth x 6.4mm Diam., Cap Side Arm 2.7mm O.D. x 1.4mm I.D. (F8)

Device Record Status

Public Device Record Key: 81172e33-6fde-4d4c-a4af-2aa2e5c8d94f
Public Version Date: February 20, 2025
Public Version Number: 2
DI Record Publish Date: April 03, 2020