AccessGUDID - DEVICE: Hayden Medical (00840319716632)

GUDID

Device Identifier (DI) Information

Brand Name: Hayden Medical
Version or Model: OP23-012
Commercial Distribution Status: In Commercial Distribution
Catalog Number: OP23-012
Company Name: Hayden Medical, Inc.

Primary DI Number: 00840319716632
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 618214410 *Terms of Use

Device Description: Large Synthetic Latex Free Rubber Suction Cups, autoclavable, one dozen

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:	No
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?
63962	Corneal shield applicator	A hand-held manual device designed to place a shield on a patient’s cornea for protection during a medical procedure (e.g., periorbital surgery, dermatological laser treatment). It is typically in the form of a soft bulb or cup that when squeezed creates gentle suction against the shield, enabling the user to lift the shield and then gently position it on the patient’s cornea. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KYE	Inserter/remover contact lens

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: No
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

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: 23d71a1f-a14c-4365-9741-00c34c0830b2
Public Version Date: August 11, 2022
Public Version Number: 1
DI Record Publish Date: August 03, 2022

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

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: No
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1(661)296-7200
Email: info@haydenmedical.com

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