FDA.reportPublic FDA data

VACUTRON

Primary DI
00260720009138
Brand
VACUTRON
Company
ALLIED HEALTHCARE PRODUCTS, INC.
Model
MINI-VAC
Catalog number
22-16-1108-G
Device description
INTERMITTENT SUCTION REGULATORS
Published
2016-09-09
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
false

Product Codes#

Code, Name table
CodeName
KDPRegulator, Vacuum

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KDPRegulator, VacuumGeneral Hospital2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00260720009138PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00260720009138002607200091382607200091380260720009138

GMDN Terms#

Term, Definition table
TermDefinition
General-purpose suction system, vacuumAn assembly of devices designed to evacuate fluid, tissue, gas, or foreign materials from a body cavity or lumen by means of suction. It is connected via dedicated vacuum tubing to the vacuum terminal unit (wall outlet) of a vacuum pipeline system and powered via a hospital's central vacuum system. It generally includes a regulator, tubing, an overflow trap, plastic/glass collection container(s), a suction tip, and possibly moisture/microbial filters. The regulator controls the vacuum in the suction tubing for the removal of materials into the collection container. This system can be used in a wide variety of hospital settings, but is limited to connection to a central vacuum system.

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

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
08435510679101TITANIUM VAC REGHERSILL SLKDP2026-01-07
08435510679767TITANIUM VAC REGHERSILL SLKDP2026-01-07
08435510679774TITANIUM VAC REGHERSILL SLKDP2026-01-07
08435510679866TITANIUM VAC REGHERSILL SLKDP2026-01-07
08435510679873TITANIUM VAC REGHERSILL SLKDP2026-01-07
08435510680039TITANIUM VAC REGHERSILL SLKDP2026-01-07
08435510680046TITANIUM VAC REGHERSILL SLKDP2026-01-07
08435510680053TITANIUM VAC REGHERSILL SLKDP2026-01-07
00850027043814Precision MedicalPrecision Medical, Inc.KDP2026-01-05
10197344143757MEDLINEMEDLINE INDUSTRIES, INC.KDP2025-12-12
10197344143580MEDLINEMEDLINE INDUSTRIES, INC.KDP2025-08-14
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10197344143610MEDLINEMEDLINE INDUSTRIES, INC.KDP2025-08-14
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10197344098996MEDLINEMEDLINE INDUSTRIES, INC.KDP2024-07-11