← Back to catalogue

Aesculap

FDA UDI

Class II (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
AESCULAP FDA UDI
Generic Name
Laparoscopic access cannula, reusable FDA UDI
Device Name
FLEXIBLE CANNULA 7MM 100MM LENGTH FDA UDI
Model / Reference
EJ806P FDA UDI
Description
FLEXIBLE CANNULA 7MM 100MM LENGTH FDA UDI

Identifiers

Catalog Number
EJ806P FDA UDI
Primary DI / UDI-DI
04038653152995 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Laparoscopic access cannula, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 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

No

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 access cannula, reusable

Aesculap by Aesculap, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laparoscopic access cannula, 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

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI 6ea15f12-734b-444d-9d22-6e60d62a3a91 36 fields · synced May 30, 2026