Ambler Surgical - Sideport/Groove diamond knife, straight, 1.00mm - AMBLER SURGICAL CORP.

Duns Number:015272206

Device Description: Sideport/Groove diamond knife, straight, 1.00mm wide, tri-square blade, sharp sides, micro Sideport/Groove diamond knife, straight, 1.00mm wide, tri-square blade, sharp sides, micrometer titanium handle, 10 micron increments, 1.5mm max blade extension

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More Product Details

Catalog Number

27-651E

Brand Name

Ambler Surgical

Version/Model Number

Sideport/Groove diamond knife

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

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)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

HNN

Product Code Name

Knife, ophthalmic

Device Record Status

Public Device Record Key

bafcd514-52c2-4bf7-81b4-76241afb0efd

Public Version Date

January 12, 2021

Public Version Number

1

DI Record Publish Date

January 04, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"AMBLER SURGICAL CORP." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 14984
2 A medical device with a moderate to high risk that requires special controls. 3118