Dale Transducer Holder 620

GUDID H84106202

Dale Transducer Holder, Fits most

DALE MEDICAL PRODUCTS, INC.

Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use Electrode/transducer strap, single-use

• Primary Device ID: H84106202
• NIH Device Record Key: 80563159-e585-4e8a-88ec-649119a23c9e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dale Transducer Holder
• Version Model Number: 620
• Catalog Number: 620
• Company DUNS: 001061233
• Company Name: DALE MEDICAL PRODUCTS, 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: 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: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	H84106201 [Primary]
HIBCC	H84106202 [Package]; Contains: H84106201; Package: Box [10 Units]; In Commercial Distribution

FDA Product Code

• KGX: Tape And Bandage, Adhesive

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-03-13
• Device Publish Date: 2018-08-29

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