Hays Inc.

Primary DI
00860003700822
Brand
Hays Inc.
Company
HAYS, INC.
Model
HS1500AS
Catalog number
HS1500AS
Device description
Hays Innovations Anchor Sound Device
Published
2020-06-02
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
OTC
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
KKXDrape, Surgical

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KKXDrape, SurgicalGeneral, Plastic Surgery2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K101689000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K101689000EMM EQUIPMENT COVER-POLYTHYLENEExact Medical Manufacturing, Inc.2010-09-20KKX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00860003700839PackageGS120In Commercial Distribution
00860003700846PackageGS16In Commercial Distribution
00860003700822PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00860003700839008600037008398600037008390860003700839
00860003700846008600037008468600037008460860003700846
00860003700822008600037008228600037008220860003700822

GMDN Terms#

Term, Definition table
TermDefinition
Medical equipment/instrument drape, single-useA flexible polymer sheet/bag/sleeve designed to form a protective water-resistant enclosure around a piece of medical equipment/instrument (e.g., C-arm, surgical laser/camera/microscope, examination table/chair) and/or components (e.g., cables, tubes, headrest). It is intended as a hygienic barrier to protect the equipment/instrument from soiling and/or contamination when used inside, or within the vicinity of, a hygienic area; it may have patient contact, however it is not intended to be introduced into a body cavity (noninvasive). It is neither a dedicated handle cover, device cap nor an ultrasound transducer cover. This is a single-use device.

Regulatory Flags#

DUNS number
079906040
Device count
1
Lot or batch
true
Expiration date on label
true
No natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00869566000233Hays InnovationsH1000EH1000SE2016-09-09
00869566000271Hays IncHS2000HLHS2000HL2020-03-30
00860003700839Hays Inc.HS1500ASHS1500AS2020-06-02
00860003700853Hays IncHS2100SSHS2100SS2021-02-04
00860003700860Hays IncHS2100SSHS2100SS2021-02-04
00860003700808Hays IncHS2000HLHS2000HL2020-03-30
20869566000237Hays InnovationsH1000EH1000SE2016-09-09
00869566000240Hays InnovationsH1000SH1000S2016-09-09
00869566000202Hays InnovationsE632203NEO-01NE632203NEO-01N2016-09-09
00869566000264Hays InnovationsH1000SH1000S2016-09-09

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Primary DI, Brand, Company table
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08056646500291Basic Implant SetOMNIA SRLKKX2026-03-27
08056646500307Implantology SetOMNIA SRLKKX2026-03-27
08056646500321Oral Surgery SetOMNIA SRLKKX2026-03-27
08056646500482Oral Surgery PackOMNIA SRLKKX2026-03-27
10812564036022MedlineMEDLINE INDUSTRIES, INC.KKX2026-03-11
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