Responder

GUDID 00841492101932

RAULAND-BORG CORPORATION

Nurse call system

• Primary Device ID: 00841492101932
• NIH Device Record Key: c28f18f0-72b5-4f72-98a0-03145375d606
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Responder
• Version Model Number: R4K11V
• Company DUNS: 005105515
• Company Name: RAULAND-BORG CORPORATION
• 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: 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	00841492101932 [Primary]

FDA Product Code

• OUG: Medical Device Data System

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-06-02
• Device Publish Date: 2017-11-21

On-Brand Devices [Responder]

• 00841492104681: 354017
• 00841492104490: 354001
• 00841492104476: 354000
• 00841492104438: 353100
• 00841492104384: 353001
• 00841492104308: 352000
• 00841492104285: 351310
• 00841492104186: 351004
• 00841492103899: 3225300
• 00841492102526: R5KUCNL
• 00841492102441: R5KPS1A
• 00841492102175: R5KDC016
• 00841492102083: R5KANN
• 00841492101949: R4K12A
• 00841492101932: R4K11V
• 00841492101833: R4KSS
• 00841492101826: R4KSR1
• 00841492101819: R4KSPK
• 00841492101789: R4KSAR
• 00841492101680: R4KPC10
• 00841492101666: R4KPB23
• 00841492101352: R4KANNV2
• 00841492101116: NCUS1
• 00841492100881: NCLCD
• 00841492100829: NCDUTY
• 00841492100416: DCV100
• 00841492100232: CLA246
• 00841492102496: R5KSMST
• 00841492102090: R5KAUDPC