Alpine SL

GUDID 00885797695284

ROTH ALPINE SL 022 HK/345 5-5 20 EA

Rmo, Inc.

Orthodontic bracket, metal

• Primary Device ID: 00885797695284
• NIH Device Record Key: 852d5241-92aa-4ee3-9bf7-f2ee51583048
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Alpine SL
• Version Model Number: KM22402
• Company DUNS: 007058183
• Company Name: Rmo, 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: 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	00885797695284 [Primary]

FDA Product Code

• EJF: Bracket, Metal, Orthodontic

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: 2024-09-10
• Device Publish Date: 2024-09-02

On-Brand Devices [Alpine SL]

• 00885797714596: BIO ALPINE SL DOLICHOFACIAL 018 HK/3 5-5 20 EA
• 00885797714589: BIO ALPINE SL MESOFACIAL 018 HK/3 5-5 20 EA
• 00885797714572: BIO ALPINE SL BRACHYFACIAL 018 HK/3 5-5 20 EA
• 00885797695284: ROTH ALPINE SL 022 HK/345 5-5 20 EA
• 00885797695277: MBT ALPINE SL 022 HK/345 5-5 20 EA