Remel Inc- Buffered Peptone Water

GUDID 00842558115306

Buffered Peptone Water

REMEL, INC.

Culture medium base ingredient IVD

• Primary Device ID: 00842558115306
• NIH Device Record Key: d87c38bf-4e46-47bd-95c2-88935a85020e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Remel Inc- Buffered Peptone Water
• Version Model Number: R112133
• Company DUNS: 065769564
• Company Name: REMEL, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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	00842558115306 [Primary]

FDA Product Code

• LIB: Device, General Purpose, Microbiology, Diagnostic

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-09-08
• Device Publish Date: 2023-08-31

Devices Manufactured by REMEL, INC.

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• 00848838058455 - Remel™ RapID™ ERIC™ (ELECTRONIC RAPID IDENTIFICATION COMPENDIUM): 2024-11-21
• 00848838003240 - REMEL: 2024-11-07 Tergitol 7 Agar w/TTC 10/PK
• 00848838007736 - REMEL: 2024-11-07 Lysozyme Broth (5ml) 20/PK
• 00842558116419 - ACT I Transport PK/10: 2024-08-14
• 00842558116426 - ACT II Transport PK/10: 2024-08-14
• 00842558116433 - ACT II Dual Transport PK/10: 2024-08-14
• 05032384519903 - ProSpecT: 2024-08-06 ProSpecT C. diff Toxin A/B MP KT/96TST