AccessGUDID - DEVICE: ONE (03700483624522)

GUDID

Device Identifier (DI) Information

Brand Name: ONE
Version or Model: ONE-DEEP WELL FULL CUT D7.75MM X 1
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 17214D775
Company Name: MORIA SA

Primary DI Number: 03700483624522
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 275937506 *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":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
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?
47088	Corneal punch set	A collection of surgical instruments intended to cut a precise circular section of the cornea (corneal button) from stored cadaveric donor tissue for transplantation into a prepared patient. It typically consists of a small base plate, an extremely sharp and hollow cylinder that has a thin circular cutting edge (a trephine), and a guide through which the trephine can travel. The surgeon typically places a section of corneal tissue into the centre of the base plate (it has a graduated inverse bowl emulating the curvature of the eye), assembles the guide and trephine into position, and applies pressure onto the trephine to cut the button. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HNJ	Punch, Corneo-Scleral

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: 296f1804-cff6-4c60-9c84-868db875f359
Public Version Date: January 05, 2024
Public Version Number: 1
DI Record Publish Date: December 28, 2023

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
03700483624539	1	03700483624522		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: No
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: Yes
Donation Identification Number: No CLOSE

Customer Contact

[?]

No Customer Contact currently defined

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