← Back to catalogue

C35-Scalpel accessory tool

FDA UDI

Class I (US FDA UDI)

by Medica Corp.

Identity

Trade Name
C35-Scalpel accessory tool FDA UDI
Generic Name
Laparoscopic surgical procedure kit, non-medicated, reusable FDA UDI
Model / Reference
C35-SAT-2 FDA UDI

Identifiers

Catalog Number
C35-SAT-2 FDA UDI
Primary DI / UDI-DI
E496C35SAT20 FDA UDI
FDA Product Code
GDX FDA UDI
GMDN Term
Laparoscopic surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

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 surgical procedure kit, non-medicated, reusable

C35-Scalpel accessory tool by Medica Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laparoscopic surgical procedure kit, non-medicated, 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
Medica Corp.

Sources (1)

  • FDA UDI a03f8c51-faa8-48cd-b73b-57fef152fee2 33 fields · synced Jun 8, 2026