Device
ResMed Astral Inlet Filter - 2/PK
Manufacturer
SUNSET HEALTHCARE SOLUTIONS, INC.
Model: VF003-2 DI: 00848530108946 Status: New MRI: Labeling does not contain MRI Safety Information Single-use: Yes Rx: No OTC: No
First Published: 2026-04-30 Current Version: 2026-05-08
Description
ResMed Astral Inlet Filter - 2/PK
Sterilization
Device Sterile: No
Sterilization Prior To Use: No
Regulatory & Distribution
Record Status: Published
Version Number: 1
Record Key: d24410a1-519c-49f9-9c3e-b309332a3cb3
Distribution Status: In Commercial Distribution
DUNS Number: 141668116
Device Count: 1
DM Exempt: No
Premarket Exempt: Yes
HCT/P: No
Kit: No
Combination Product: No
Lot/Batch Tracked: Yes
Serial Number Tracked: No
Manufacturing Date Tracked: No
Expiration Date Tracked: No
Donation ID Number Tracked: No
Labeled Contains NRL: No
Labeled No NRL: No
Identifiers
Device ID: 00848530108946
Type: Primary
Issuing Agency: GS1
GMDN
Code: 31245
Name: Local/regional anaesthesia conduction filter
Definition:
A microporous membrane used to minimize particulate (foreign material) contamination of a local anaesthetic during subcutaneous administration to a patient (e.g., through a spinal or epidural catheter); it may in addition be intended for use during medication administration or preparation. This is a single-use device.
FDA Product Codes
JRL
Unit, Filter, Membrane