AccessGUDID - DEVICE: OPTIVISOR MAGNIFIER (00192896096226)

GUDID

Device Identifier (DI) Information

Brand Name: OPTIVISOR MAGNIFIER
Version or Model: 1103-402
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 1103-402
Company Name: SONTEC INSTRUMENTS, INC.

Primary DI Number: 00192896096226
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 040729840 *Terms of Use

Device Description: OPTIVISOR MAGNIFIER #DA-3

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?
46550	Spectacle-mounted magnifier	A magnifying ophthalmic lens designed to be attached to a pair of spectacles and intended to enlarge text/images for a visually impaired patient/person. It is also known as a magnifying glass and can be made of solid plastic material or glass within a plastic or metal frame.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FSP	Loupe, Diagnostic/Surgical

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: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: 1.75 Magnification at 14 Inches

Device Record Status

Public Device Record Key: 232f83cf-f7fa-4ef3-8ff9-a18cb6a3275b
Public Version Date: June 12, 2019
Public Version Number: 3
DI Record Publish Date: May 08, 2019

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: 800-821-7496
Email: info@sontecinstruments.com

MENU
- Home
- About
- News
- API
- Download
- Help

FDA TOOLS & RESOURCES