Post Medical, Inc.

GUDID B309WD1501

POST MEDICAL, INC.

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• Primary Device ID: B309WD1501
• NIH Device Record Key: 9afe6744-dbad-4fca-881d-c41dff3f05b3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Post Medical, Inc.
• Version Model Number: WD-150
• Company DUNS: 968012943
• Company Name: POST MEDICAL, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B309WD1500 [Primary]
HIBCC	B309WD1501 [Package]; Contains: B309WD1500; Package: Case [24 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K925816

FDA Product Code

• FMI: Needle, Hypodermic, Single Lumen

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-20

On-Brand Devices [Post Medical, Inc.]

• B309WD200Y1: WD200Y
• B309WD2000: WD-200
• B309WD1501: WD-150
• B309WD1101: WD-110
• B309SL2001: SL-200
• B309SL1501: SL-150
• B309SL1001: SL-100
• B309PMSM9501: PMSM-950
• B3093G1: 3G
• B3093301LPR1: 3301-LPR
• B3092GY1: 2GY
• B3092G1: 2G
• B3092201LPR1: 2201-LPR
• B3092201LPBWY1: 2201-LPBW-Y
• B3092201LPBW1: 2201-LPBW
• B3091G1: 1G
• B3091101LPR0: 1101LPR
• B3091101LPBW0: 1101-LPBW