TL 1000 - Examination Light

GUDID 00887761968349

TruLight 1000 / Mobile

Baxter Medical Systems GmbH + Co. KG

Fixed examination/treatment room light

• Primary Device ID: 00887761968349
• NIH Device Record Key: 49896efc-88f9-4e28-b9ec-b4f2d9080254
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TL 1000 - Examination Light
• Version Model Number: 4058130
• Company DUNS: 330961223
• Company Name: Baxter Medical Systems GmbH + Co. KG
• 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

Customer Support Contacts

• Phone: +4936715860
• Email: SURGICAL@HILLROM.COM
• Phone: +4936715860
• Email: SURGICAL@HILLROM.COM
• Phone: +4936715860
• Email: SURGICAL@HILLROM.COM
• Phone: +4936715860
• Email: SURGICAL@HILLROM.COM
• Phone: +4936715860
• Email: SURGICAL@HILLROM.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887761968349 [Primary]

FDA Product Code

• KZF: Device, medical examination, ac powered

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: 2023-02-09
• Device Publish Date: 2022-12-15

On-Brand Devices [TL 1000 - Examination Light]

• 00887761968363: TruLight 1000 / ceiling
• 00887761968356: TruLight 1000 / wall
• 00887761968349: TruLight 1000 / Mobile
• 00887761968332: TruLight 1000 / pendant