Allied Healthcare Products Inc.

Primary DI
00026072002483
Brand
Allied Healthcare Products Inc.
Company
ALLIED HEALTHCARE PRODUCTS, INC.
Model
13305-1
Catalog number
20-02-0153
Device description
Specimen Bag
Published
2016-09-16
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
true

Product Codes#

Code, Name table
CodeName
KDQBottle, Collection, Vacuum

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KDQBottle, Collection, VacuumGeneral Hospital2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
40026072002481PackageGS112In Commercial Distribution
00026072002483PrimaryGS10
40260720002489Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
4002607200248140026072002481
00026072002483000260720024830260720024830026072002483
4026072000248940260720002489

GMDN Terms#

Term, Definition table
TermDefinition
Suction system filter, microbialA screening device intended to be installed within a suction system and which has a membrane pore size small enough to retain bacterial pathogens, thus preventing the environment from becoming infected and decreasing the risk of cross-infection to subsequent patients. It is typically directly connected to the suction system collection bottle/canister, or as a common filter serving more than one bottle/canister through a switching mechanism, or in a tubing line between the suction bottle/canister and the suction pump, or at the suction pump exhaust where driving gases are discarded. This is a single-use device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
099674145
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
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

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00026072017999PC15008-03P2023-12-22
00026072018002PC15008-03P-A2023-12-22
00026072018019PC15008-03T2023-12-22
00026072018026PC15008-03T-A2023-12-22
00026072018033PC15008-03TP22023-12-22
00026072018040PC15008-03TP2-A2023-12-22
00026072018057PC15008-03Y2023-12-22
00026072018064PC15008-03Y-A2023-12-22
00026072018071PC15008-03YP12023-12-22
00026072018088PC15008-03YP1-A2023-12-22
00026072018095PC15008-03YP22023-12-22
00026072018101PC15008-03YP2-A2023-12-22
00026072018118PC15008-132023-12-22
00026072018125PC15008-13-A2023-12-22
00026072018132PC15008-13P2023-12-22
00026072018149PC15008-13P-A2023-12-22
00026072018156PC15008-13T2023-12-22
00026072018163PC15008-13YP2-A2023-12-22
00026072018170PC15009-032023-12-22
00026072018187PC15009-03-A2023-12-22

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