GUDID 04719873698240

CariRaise M-Set 20" x 75" TDX Carilex

CARILEX MEDICAL, INC.

Alternating-pressure bed mattress overlay system

• Primary Device ID: 04719873698240
• NIH Device Record Key: 925cb8f9-b497-49ce-a5bd-e9a023407000
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: S2106-2010
• Company DUNS: 658863238
• Company Name: CARILEX MEDICAL, 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: false
• Serial Number: true
• Manufacturing Date: true
• 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
GS1	04719873698240 [Primary]

FDA Product Code

• FNM: Mattress, Air Flotation, Alternating Pressure

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: 2025-08-06
• Device Publish Date: 2025-07-29

Devices Manufactured by CARILEX MEDICAL, INC.

• 04719873698240 - NA: 2025-08-06CariRaise M-Set 20" x 75" TDX Carilex
• 04719873698240 - NA: 2025-08-06 CariRaise M-Set 20" x 75" TDX Carilex
• 04719873698233 - NA: 2025-07-28 Centrius P.U. US Carilex for CariRaise
• 04719873698226 - NA: 2025-07-17 VT•100/VT•200 Carrying Bag for 1000ml Canister Carilex-1p
• 04719873698172 - NA: 2025-06-27 CariRaise SYS US Carilex (L type)
• 04719873698189 - NA: 2025-06-27 CariRaise SYS US Carilex (R type)
• 04719873696901 - NA: 2024-06-28 TheraFlo 9 M-set 36" x 80" WDTX Carilex
• 14719873696915 - NA: 2024-06-28 TheraFlo 9 Cover 36" x 80" WDTX Carilex-1p
• 04719873696925 - NA: 2024-06-28 TheraFlo 9 M-set 42" x 80" DTX Carilex