Welmed, Inc.

Primary DI
00849296003353
Brand
Welmed, Inc.
Company
WELMED INC.
Model
1501-1018
Device description
Instrument Pouch w/ 2 pockets, Sterile, 1 each/pouch, 10 pouches/box, 4 boxes/case
Published
2017-06-14
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
PUIDrape, Surgical, Exempt

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
PUIDrape, Surgical, ExemptGeneral, Plastic Surgery2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10849296003350PackageGS110In Commercial Distribution
20849296003357PackageGS14In Commercial Distribution
00849296003353PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1084929600335010849296003350
2084929600335720849296003357
00849296003353008492960033538492960033530849296003353

GMDN Terms#

Term, Definition table
TermDefinition
Surgical instrument interim-placement holder, single-useA device intended to be used in the operating room (OR) by staff to safely hold a hand-held, manual, surgical instrument(s) [e.g., needle, scalpel, scissors, robotic system instrument hand-held remote controller] when not in use during surgery, to avoid damage to the instrument, maintain its sterility, and/or for temporary storage (e.g., to enable easy transfer/handling of the instrument at reduced risk of injury). It is available in various forms (e.g., rack, puncture cushion, telescopic tube, magnetic mat), and may be attached to a surgical drape; it is not a numbered tray and is not intended for counting of sharps. This is a single-use device.

Sterilization Methods#

Method table
Method
Ethylene Oxide

Regulatory Flags#

DUNS number
828213426
Device count
1
Premarket exempt
true
Lot or batch
true
Expiration date on label
true
No natural rubber latex
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00849296017107Welmed, Inc.IOT-CDS122026-03-26
00849296004916Welmed, Inc.1222-86522026-03-20
00849296002790Welmed, Inc.1222-86662017-06-14
00849296013345Welmed1300-01TB2026-02-15
00849296013352Welmed1300-02LL2026-02-15
00849296013369Welmed1300-03LL2026-02-15
00849296013376Welmed1300-03LS2026-02-15
00849296013383Welmed1300-05LL2026-02-15
00849296013390Welmed1300-05LS2026-02-15
00849296013406Welmed1300-06LL2026-02-15
00849296013413Welmed1300-10CNTL2026-02-15
00849296013420Welmed1300-10LL-8002026-02-15
00849296013437Welmed1300-10LS2026-02-15
00849296013444Welmed1300-12LL2026-02-15
00849296013451Welmed1300-20LL2026-02-15
00849296013475Welmed1300-30LL2026-02-15
00849296013482Welmed1300-30LS2026-02-15
00849296013499Welmed1300-60LL2026-02-15
00849296013505Welmed1300-60LS2026-02-15
00849296009898Welmed1923-4040LFST2026-02-15

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