FDA.report

Welch Allyn, Inc.

Primary DI
00732094075816
Brand
Welch Allyn, Inc.
Company
WELCH ALLYN, INC.
Model
901038
Catalog number
MIL5062
Device description
Welch Allyn English MacIntosh and Miller 2.5 V Halogen HPX Fiber-Optic Laryngoscope Set; Green Standard (ISO 7376), Stainless Steel, E-Mac Blade Size #1 to #4 (Qty. 4), Miller Blade Size #0 to #4 (Qty. 5), Medium C-Cell Power Handle, Small AA-Cell Power Handle, Stubby AA-Cell Power Handle, Hard Storage Case, Replacement HPX Lamps and Lamp-Cartridge
Published
2023-08-17
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Related Records

Contact Domains

Product Codes

CodeName
CCWLARYNGOSCOPE, RIGID

Product Code Classifications

CodeDeviceSpecialtyClass
CCWLaryngoscope, RigidAnesthesiology1

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00732094075816PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
00732094075816007320940758167320940758160732094075816

GMDN Terms

TermDefinition
Blood pressure cuff, reusableA band-like device that has an inflatable bladder in an inelastic sleeve with one or two connecting tubes with connector (typically locking connectors) that can be connected to a mechanism for inflating and deflating the bladder and/or a sphygmomanometer or a patient monitoring device/system that is used to determine a patient's blood pressure. It is wrapped around the upper arm or the leg (thigh) of the patient. This is a reusable device which may be intended for single-patient or multi-patient reuse.

Sterilization Methods

Method

Contacts

PhoneEmail
+1(315)685-2834GDSN_SUPPORT@MYHILLROM.ONMICROSOFT.COM

Regulatory Flags

DUNS number
198227881
Device count
1
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
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

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