Sterimed

Primary DI
00860001790207
Brand
Sterimed
Company
STERIMED LLC
Model
0888NT
Catalog number
0888NT
Device description
"Equipment Drape 18"" X 24"" "
Published
2019-05-16
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

Contact Domains#

Product Codes#

Code, Name table
CodeName
IZISystem, X-Ray, Angiographic

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
IZISystem, X-Ray, AngiographicRadiology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K853044000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K853044000STERICOVERSterimed, Inc.1985-11-01IZI

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10860001790204PackageGS1100In Commercial Distribution
00860001790207PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1086000179020410860001790204
00860001790207008600017902078600017902070860001790207

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.

Sterilization Methods#

Method table
Method
"[""Radiation Sterilization"", ""Ethylene Oxide""]"

Contacts#

Phone, Email table
PhoneEmail
770-387-0771XX@XX.XX

Regulatory Flags#

DUNS number
080284658
Device count
1
Lot or batch
true
No natural rubber latex
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
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00850341007370SterimedMR00822016-09-19
00850341007387SterimedMR01202016-09-19
00850341007394SterimedPB10032016-09-19
00850341007479SterimedWG01052016-09-19
00850341007486SterimedWR01202016-09-19
00850341007493SterimedWR01502016-09-19
00850341007509SterimedWR10102016-09-19
00850341007516SterimedZB10052016-09-19
00850341007523SterimedZG00822016-09-19
00850341007752SterimedMR01502016-09-19
00850341007776SterimedTR0105B2016-09-19
00850341007790SterimedZB00962016-09-19
00850341007806SterimedZG10012016-09-19
00850341007813SterimedZG10062016-09-19
00850341007905SterimedZG10072016-09-19
00860001790214Sterimed3520SB2020-04-27
00860001790290SterimedBD921262021-09-29

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