Liquid Stuarts,Wire Shaft PK/50

GUDID 00848838066931

REMEL, INC.

General specimen collection kit

• Primary Device ID: 00848838066931
• NIH Device Record Key: 968a743f-5f1a-4573-b70c-43c05a3a7130
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Liquid Stuarts,Wire Shaft PK/50
• Version Model Number: R723135
• Company DUNS: 065769564
• Company Name: REMEL, 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: true
• Expiration Date: true
• 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
GS1	00848838066931 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K943499

FDA Product Code

• JSM: Culture Media, Non-Propagating Transport

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-06-26
• Device Publish Date: 2025-06-18

Devices Manufactured by REMEL, INC.

• 00842558116709 - Spectra™ Candida Agar: 2026-02-17
• 00848838072772 - MicroTest M6: 2026-02-17 M6 (1.5ml) Universal Swab Kit PK/100
• 00848838074844 - MicroTest M4RT: 2026-02-17 M4RT(3ml) Universal Flock Swab Kit PK/100
• 00848838075018 - MicroTest M6: 2026-02-17 M6(1.5ml) Traditional FlockSwab KitPK/100
• 00848838091742 - VersaTREK™: 2026-02-04
• 00848838003158 - Strep Selective II Agar: 2026-01-26
• 00848838059865 - ^BM^ PK/50 OXIDASE TEST: 2026-01-26 ^BM^ PK/50 OXIDASE TEST
• 00842558116402 - BactiSwab Dry PK/100: 2025-06-27