Miller фибер optic Ларингоскоп Лезвия 65m -70mm (Ref DI 01-20-01)

$ 0

Miller фибер optic Ларингоскоп Лезвия 65m -70mm :

Наша новая, инновационная технология производства обеспечивает еще лучшее освещение и более длительный срок службы. Мы можем изготовить ваш продукт с высококачественным стандартным сырьем.

MOQ: 50 pieces
Lead time: 18–22 working days
Sample order: 10 units · sample fee credited against first PO
OEM private label: Private-label from 300 units per SKU
Materials: AISI 303 / AISI 304 stainless steel (AISI 316 on fiber-optic variants)
Sterilization: Steam autoclave to 134 °C · EtO compatible
Certifications: ISO 13485:2016 · CE-marked under EU MDR 2017/745 · FDA establishment-registered
Shipping: DHL Express · UPS · FedEx · sea freight · all Incoterms

Need a different size, custom branding, or volume pricing?
Request a quote →

SKU DI 01-20-01 Category
Regulatory Nomenclature
EMDN (EUDAMED): V0303100201
GMDN Code: 35192
Laryngoscope blade, rigid, reusable

Fizza Surgical supplies the Miller фибер optic Ларингоскоп Лезвия 65m -70mm (Ref DI 01-20-01) as a standard catalogue line to hospitals and distributors.

The Miller laryngoscope blade — developed by American anaesthetist Robert A. Miller in 1941 — is the straight blade used primarily for paediatric and difficult-airway intubation. Where Macintosh’s curved tip sits in the vallecula and indirectly lifts the epiglottis, the Miller’s straight blade is placed directly under the epiglottis and lifts it forward. This direct technique provides better laryngeal exposure in infants (whose epiglottis is large and floppy) and in difficult adult intubations where the Macintosh fails. Miller blades are manufactured in sizes 0 (neonatal) through 4 (large adult), with sizes 0, 1, and 2 most used in paediatric anaesthesia.

Reference / SKUDI 01-20-01
PatternMiller
Working length70 mm (7 cm)
MaterialAISI 303 / AISI 304 stainless steel (AISI 316 on fiber-optic variants)
SterilizationSteam autoclave to 134 °C · EtO compatible
Quality systemISO 13485:2016 · CE-marked under EU MDR 2017/745 · FDA establishment-registered

Fizza Surgical International has manufactured surgical instruments at its Sialkot, Pakistan facility since 1980 — more than four decades of continuous operation under one family ownership. The factory holds ISO 13485:2016 certification for medical devices and CE marking under EU MDR 2017/745, the regulatory baseline European hospitals and distributors require. FDA establishment registration covers exports to the United States.

What is the minimum order quantity for Fizza Surgical instruments?
Standard MOQ is 300 units per SKU for catalogue items, 500 units for fully custom designs. Sample orders of 10 units per SKU are available with the sample fee credited against the first production order.
Are Fizza Surgical instruments CE-marked and ISO 13485 certified?
Yes. All instruments are manufactured under an ISO 13485:2016 Quality Management System, CE-marked under EU MDR 2017/745, and our facility is FDA-registered. Specific certificate numbers and PDFs are on our Certifications page.
How long is the lead time and what shipping options are available?
18–22 working days for catalogue items, 28–35 days for custom designs. Shipping via DHL Express, UPS, FedEx, or sea freight on all standard Incoterms (EXW, FCA, FOB, CIF, DAP).
Can I order a custom OEM private-label run with my own branding?
Yes — private-label manufacturing from 300 units per SKU. Co-branded packaging, custom instrument-set design, and laser etching with your brand are all available.

Reviews

There are no reviews yet.

Only logged in customers who have purchased this product may leave a review.

Serving 50+ countries in 7 languages View Global Markets
Scroll to Top
WhatsApp
Fizza Surgical
Fizza Surgical ● Online — typically replies instantly