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Bladeless Trocar - Artemis Lap™ Cannula Depth Limiter Ø12mm

FDA UDI

Class II (US FDA UDI)

by T.a.g Medical Products Agricultural Cooperative Association

Identity

Trade Name
Bladeless Trocar - Artemis Lap™ Cannula Depth Limiter Ø12mm FDA UDI
Generic Name
Laparoscopic access cannula, single-use FDA UDI
Model / Reference
157210et FDA UDI

Identifiers

Catalog Number
157210et FDA UDI
Primary DI / UDI-DI
10818674029732 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscopic access cannula, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Laparoscopic access cannula, single-use

Bladeless Trocar - Artemis Lap™ Cannula Depth Limiter Ø12mm by T.a.g Medical Products Agricultural Cooperative Association — Class II — FDA UDI — listed in…

Similar devices

Also classified as Laparoscopic access cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a6bfda5e-ad21-4cf5-96ee-31b33ae12667 33 fields · synced May 30, 2026