TEST IT

Device

EU IVDD · Eu Ivd Annex 2 List A ·TÜRKLAB TIBBİ MLZ. SAN. VE TİC. AŞ.·On the market

FSSB

FDA UDI

Surgical Specialties México, S. de R.L. de C.V.·00848782029631·DLZ-6.4-200 8-0 Bl V Silk 18"/45 Cm

ILA(INVERTED LINEAR ANASTOMOSIS) STAPLER

FDA 510(k)

FDA Class 2 ·General Hospital

ALZ WEB PACS, VERSION 1.0

FDA 510(k)

FDA Class 2 ·Radiology

FSSB

FDA UDI

Surgical Specialties México, S. de R.L. de C.V.·00848782039036·DLZ-6.4-200 USP 7/0 PGA violet 30 cm. sterile V...

LORCA MARIN

FDA UDI

Surgical Specialties México, S. de R.L. de C.V.·00848782039203·DLZ-6.2-150 USP 10/0 Nylon black 15 cm. sterile...

FSSB

FDA UDI

Surgical Specialties México, S. de R.L. de C.V.·00848782038862·DLZ-6.4-200 USP 10/0 Nylon black 15 cm. sterile...

LORCA MARIN

FDA UDI

Surgical Specialties México, S. de R.L. de C.V.·00848782039234·DLZ-5.6-150 USP 8/0 Nylon black 15 cm. sterile ...

FSSB

FDA UDI

Surgical Specialties México, S. de R.L. de C.V.·00848782039074·DLZ-6.2-150 USP 10/0 PGA violet 15 cm. sterile ...

BIOFIRE FILMARRAY TF Panel

FDA registration

BioFire Diagnostics, LLC·1 product·🇺🇸 United States

BIOFIRE FILMARRAY TF Panel

FDA registration

BioFire Defense, LLC·1 product·🇺🇸 United States

BioFire Global Fever Panel

FDA registration

BioFire Defense, LLC·1 product·🇺🇸 United States

HYDROTRACK

FDA 510(k)

FDA Class 1 ·Physical Medicine

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·CONTAK RENEWAL

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·INSIGNIA/NEXUS, PRIZM/VITALITY & CONTAK RENEWAL FAMILIES

Onatec

FDA UDI

Surgical Specialties México, S. de R.L. de C.V.·00848782005406·Onasorb 1 arm(s) DLZ-6,4-200 8/0 30 cm PGA violet

FSSB

FDA UDI

Surgical Specialties México, S. de R.L. de C.V.·00848782042548·GLZ-16.0-150 USP 10-0 Polypropylene blue 10 cm ...

Onatec

FDA UDI

Surgical Specialties México, S. de R.L. de C.V.·00848782005376·Onasorb 1 arm(s) DLZ-6,4-200 7/0 30 cm PGA violet

Autolékárnička velikost I. CZ, náplň

Device

EU MDR · Eu Md Class 1 ·On the market

Medi Grade

FDA registration

FBGC LIMITED·1 product·🇬🇧 United Kingdom