Home GUDID 05707480024476 Head Wedge™
Primary DI 05707480024476
Brand Head Wedge™
Company Ambu A/S
Model 000264036
Catalog number 000264036
Device description Cervical Immobilization Device
Published 2022-12-08
Public version status Update
Distribution status In Commercial Distribution
MRI safety MR Safe
Rx false
OTC true
Sterile false
Single use true
Product Codes# Code, Name table Code Name CCX SUPPORT, PATIENT POSITION
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class CCX Support, Patient Position Anesthesiology 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 05707480006373 Package GS1 10 In Commercial Distribution 05707480024476 Primary GS1 0 05707480024483 Unit of Use GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 05707480006373 05707480006373 5707480006373 05707480024476 05707480024476 5707480024476 05707480024483 05707480024483 5707480024483
GMDN Terms# Term, Definition table Term Definition Cervical spine immobilization wedge A preformed patient-contact device (i.e., wedge) designed to be attached to a rigid flat surface (e.g., backboard) to support cervical and head immobilization during patient extrication and emergency handling. It is intended to maintain natural alignment of the head and neck by preventing lateral and rotational movement once the patient is secured to the backboard. It is typically used by emergency medical services (EMS) as part of spinal immobilization procedures. It is neither a freestanding patient positioner nor an extrication collar. This is a single-use device.
Storage And Handling# Type, Low, High table Type Low High Condition Storage Environment Temperature 0 0
Regulatory Flags# DUNS number 305682023 Device count 10 DM exempt false Premarket exempt true HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label true Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 05707480156481 aScope™ 5 Broncho 4.2/2.2 Sampler Set 620002000US 620002000US 2023-11-26 05707480157259 aScope™ 5 Broncho 4.2/2.2 620001000US 620001000US 2023-08-25 05707480157280 aScope™ 5 Broncho 2.7/1.2 624001000US 624001000US 2023-08-25 05707480167579 Ambu® Neuroline Monopolar 74225-36/40 74225-36/40 2026-09-05 05707480167593 Ambu® Neuroline Monopolar 74225-36/40 74225-36/40 2026-09-05 05707480167609 Ambu® Neuroline Monopolar 74238-36/40 74238-36/40 2026-09-05 05707480167630 Ambu® Neuroline Monopolar 74325-36/40 74325-36/40 2026-09-05 05707480167661 Ambu® Neuroline Monopolar 74338-36/40 74338-36/40 2026-09-05 05707480145287 aScope™ Duodeno 482001000 482001000 2020-08-10 05707480157402 aScope™ Duodeno 482001000/4 482001000/4 2022-04-19 05707480136032 Isiris™ Monitor MN0001 MN0001 2018-07-30 05707480156306 aScope™ 5 Broncho HD 5.0/2.2 621001000US 621001000US 2022-08-19 05707480156337 aScope™ 5 Broncho HD 5.6/2.8 622001000US 622001000US 2022-08-19 05060038511034 Ambu® WhiteSensor 40554 40554 40554 2026-08-07 05707480024650 Ambu® Mini Perfit ACE™ 000281106 000281106 2022-12-08 05707480024674 Ambu® Immobilization Kit, with 000281161 000281161 2022-12-08 05707480026197 BlueSensor NEOXECG Electrodes NEOX-60-K/US/3 NEOX-60-K/US/3 2016-09-21 05707480024513 Ambu® Perfit Collar™ 000264201 000264201 2022-12-08 05707480024520 Ambu® Perfit Collar™ 000264202 000264202 2022-12-08 05707480024537 Ambu® Perfit Collar™ 000264203 000264203 2022-12-08
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