FDA.report

APTUS

Primary DI
07630894801747
Brand
APTUS
Company
Medartis AG
Model
A-6602.117
Catalog number
A-6602.117
Device description
Implant Case APTUS Dist. Ulna Plates 2.5
Published
2024-03-21
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Related Records

Product Codes

CodeName
HRSPlate, fixation, bone

Product Code Classifications

CodeDeviceSpecialtyClass
HRSPlate, Fixation, BoneOrthopedic2

Premarket Submissions

SubmissionSupplement
K223853000

Premarket Details

SubmissionSupplementDeviceApplicantDecision dateProduct code
K223853000Medartis APTUS® Ulna PlatesMedartis AG2023-03-30HRS

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
07630894801747PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedEAN-13
07630894801747076308948017477630894801747

GMDN Terms

TermDefinition
Device sterilization/disinfection container, reusableA receptacle designed to hold wrapped and/or unwrapped medical/dental devices in a chemical washer/disinfector and/or sterilizer during the washing/disinfection and/or sterilization cycle(s). It may be designed as a tray to allow full or partial immersion of the devices in a liquid disinfectant, or as an enclosed box to prevent contamination once the sterilization process is finished. The container may also be used for transport and storage of the processed devices, and may have features such as an expiry date label, breathing filter, built-in slots or inserts to hold instruments, and stacking capabilities. This is a reusable device.

Sterilization Methods

Method
Moist Heat or Steam Sterilization

Regulatory Flags

DUNS number
480054895
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
Serial number
true
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company

Primary DIBrandModelCatalogPublished
07630894829079APTUSA-2065A-20652026-01-09
07630894829062APTUSA-2056A-20562025-12-15
07630037863670APTUSA-4750.70/1SA-4750.70/1S2025-07-31
07630037865889APTUSA-3837SA-3837S2025-07-31
07630037883791APTUSA-5800.65/1SA-5800.65/1S2025-07-31
07630037883821APTUSA-5800.70/1SA-5800.70/1S2025-07-31
07630037883852APTUSA-5800.75/1SA-5800.75/1S2025-07-31
07630037883975APTUSA-5830.40/1SA-5830.40/1S2025-07-31
07630037883999APTUSA-5830.45/1SA-5830.45/1S2025-07-31
07630037884019APTUSA-5830.50/1SA-5830.50/1S2025-07-31
07630037884033APTUSA-5830.55/1SA-5830.55/1S2025-07-31
07630037884057APTUSA-5830.60/1SA-5830.60/1S2025-07-31
07630037884071APTUSA-5830.65/1SA-5830.65/1S2025-07-31
07630037884095APTUSA-5830.70/1SA-5830.70/1S2025-07-31
07630037884101APTUSA-5830.75/1SA-5830.75/1S2025-07-31
07630037884767APTUSA-5850.65/1SA-5850.65/1S2025-07-31
07630037884798APTUSA-5850.70/1SA-5850.70/1S2025-07-31
07630037884828APTUSA-5850.75/1SA-5850.75/1S2025-07-31
07630037897125APTUSA-4350.14TPA-4350.14TP2025-07-31
07630894811784APTUSA-4340.32TPA-4340.32TP2025-07-31

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