Anodyne Surgical

Primary DI
00840516130446
Brand
Anodyne Surgical
Company
Psi/Eye-Ko, Inc.
Model
6007.2
Device description
Silicone Tip Capsule Polisher 27g X 7mm bend
Published
2023-08-24
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
true

Related Records

Contact Domains

Product Codes

CodeName
MXYCannula, Ophthalmic, Posterior Capsular Polishing, Polyvinyl Acetal

Product Code Classifications

CodeDeviceSpecialtyClass
MXYCannula, Ophthalmic, Posterior Capsular Polishing, Polyvinyl AcetalOphthalmic1

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00840516130446PackageGS150In Commercial Distribution
00840516130538PackageGS1500In Commercial Distribution
00840516130378PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
00840516130446008405161304468405161304460840516130446
00840516130538008405161305388405161305380840516130538
00840516130378008405161303788405161303780840516130378

GMDN Terms

TermDefinition
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-useA rigid or semi-rigid tube (non-illuminating) designed to be inserted into the eye to facilitate infusion, irrigation, and/or aspiration of fluids/gases during ophthalmic surgery (e.g., phacoemulsification, vitreoretinal surgery, sub-Tenon’s anaesthesia, capsule polishing). It is a single- or multi-lumen device, typically made of high-grade stainless steel, and may include a length of flexible tubing or a basic handle (without controls). It may be blunt, or include a sharp angled tip/hook (e.g., irrigating cystotome for capsulotomy), however it does not have a sharp bevelled end for initial puncture of the eye (i.e., not a needle). This is a single-use device.

Sterilization Methods

Method
Ethylene Oxide;Radiation Sterilization
Radiation Sterilization

Contacts

PhoneEmail
1(800)428-5628info@anodynesurgical.com

Regulatory Flags

DUNS number
063763833
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
true

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