AccessGUDID - DEVICE: AVID TruCustom (10809160209417)

GUDID

Device Identifier (DI) Information

Brand Name: AVID TruCustom
Version or Model: VAML043-02_0002
Commercial Distribution Status: In Commercial Distribution
Catalog Number: VAML043-02
Company Name: AVID MEDICAL, INC.

Primary DI Number: 10809160209417
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 015623119 *Terms of Use

Device Description: No description.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	Yes
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	Yes
Combination Product:	Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
57950	Ophthalmic crosslinking ultraviolet phototherapy system	A mains electricity (AC-powered) mobile device assembly, with a rechargeable battery, designed to deliver a uniform and metered dose of ultraviolet A (UVA) light to the cornea to perform an ophthalmic crosslinking procedure (collagen fibres in the cornea are linked together to stiffen the cornea). It is normally used in a clinical office setting and typically consists of a wheeled central mount that supports the optic head containing the UV source, user control panel, software, and a rechargeable battery. It is typically used to treat corneal disorders such as keratoconus, post laser assisted in situ keratomileusis (LASIK) ectasia, and other post-LASIK disorders.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
OJK	Eye tray

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 29139fe9-725c-45b1-b6ad-04ff593b207e
Public Version Date: July 14, 2025
Public Version Number: 2
DI Record Publish Date: September 13, 2018

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
20809160209414	4	10809160209417		In Commercial Distribution

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: Yes
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: Yes
Serial Number: No
Expiration Date: Yes
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1(888) 564-7153
Email: AVIDComplaints@Owens-Minor.com

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