← Back to catalogue

Ambler Surgical

FDA UDI

Class I (US FDA UDI)

by Ambler Surgical, LLC

Identity

Trade Name
Ambler Surgical FDA UDI
Generic Name
Ocular hook/spatula/manipulator, reusable FDA UDI
Device Name
Koch nucleus spatula, 4 5/8'', slightly curved, 1.0mm wide duckbill-shaped tip, round handle FDA UDI
Model / Reference
Koch nucleus spatula FDA UDI
Description
Koch nucleus spatula, 4 5/8'', slightly curved, 1.0mm wide duckbill-shaped tip, round handle FDA UDI

Identifiers

Catalog Number
6773E FDA UDI
Primary DI / UDI-DI
00190660175429 FDA UDI
FDA Product Code
HND FDA UDI
GMDN Term
Ocular hook/spatula/manipulator, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ocular hook/spatula/manipulator, reusable

Ambler Surgical by Ambler Surgical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ocular hook/spatula/manipulator, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 13cf8700-d1c0-4409-abf6-b801fe40f7e5 35 fields · synced Jun 8, 2026