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Ambler Surgical

FDA UDI

Class II (US FDA UDI)

by Ambler Surgical, LLC

Identity

Trade Name
Ambler Surgical FDA UDI
Generic Name
Laparoscopic trocar blade, reusable FDA UDI
Device Name
Laparoscopic trocar port closure/suture retriever guide cone, 2 3/8'' (6.0cm), 12.0mm diameter FDA UDI
Model / Reference
Laparoscopic trocar port closure/suture retriever guide cone FDA UDI
Description
Laparoscopic trocar port closure/suture retriever guide cone, 2 3/8'' (6.0cm), 12.0mm diameter FDA UDI

Identifiers

Catalog Number
43-952 FDA UDI
Primary DI / UDI-DI
00190660217730 FDA UDI
FDA Product Code
DRC FDA UDI
GMDN Term
Laparoscopic trocar blade, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1390 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: Laparoscopic trocar blade, reusable

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

Similar devices

Also classified as Laparoscopic trocar blade, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ambler Surgical, LLC

Sources (1)

  • FDA UDI 2d51e6b3-0aa0-4311-b66b-881c745553eb 35 fields · synced May 30, 2026