Claymount

GUDID 00871875500412

x-ray beam-limiting device, to restrict the dimensions of a diagnostic x-ray field by limiting the size of the primary x-ray beam.(Collimator) This is

Claymount Assemblies B.V.

Manual-aperture-control diagnostic x-ray system collimator, motorized

• Primary Device ID: 00871875500412
• NIH Device Record Key: 527024ef-ea28-4417-a3ee-90481c74a80e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Claymount
• Version Model Number: 50251-14-OEM
• Company DUNS: 413223942
• Company Name: Claymount Assemblies B.V.
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00871875500412 [Primary]

FDA Product Code

• IZX: Collimator, Manual, Radiographic

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: 2018-03-29
• Device Publish Date: 2017-03-15

On-Brand Devices [Claymount]

• 00871875500467: x-ray beam-limiting device, to restrict the dimensions of a diagnostic x-ray field by limiting t
• 00871875500412: x-ray beam-limiting device, to restrict the dimensions of a diagnostic x-ray field by limiting t
• 00871855000405: x-ray beam-limiting device, to restrict the dimensions of a diagnostic x-ray field by limiting t