VasoStat Hemostasis Device

Primary DI
00863879000201
Brand
VasoStat Hemostasis Device
Company
Forge Medical, Inc.
Model
10348-325-04
Device description
The VasoStat Hemostasis Device is used to augment hemostasis through a ratcheting pressuremechanism.
Published
2021-05-27
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
DXCClamp, Vascular

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DXCClamp, VascularCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K153259000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K153259000VasoStat Hemostasis DeviceForge Medical, Inc.2016-01-06DXC

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10863879000208PackageGS110In Commercial Distribution
20863879000205PackageGS11In Commercial Distribution
30863879000202PackageGS12In Commercial Distribution
40863879000209PackageGS13In Commercial Distribution
50863879000206PackageGS14In Commercial Distribution
00863879000201PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1086387900020810863879000208
2086387900020520863879000205
3086387900020230863879000202
4086387900020940863879000209
5086387900020650863879000206
00863879000201008638790002018638790002010863879000201

GMDN Terms#

Term, Definition table
TermDefinition
Radial artery compression deviceA sterile device intended to provide compression for haemostasis to the puncture site on a patient having undergone radial artery catheterization, and can be used as an alternative to direct hand pressure. It typically consists of one or more pad/strap(s), which may also have a compression/decompression knob and a time indicator; it may be applied so that it does not compress the ulna artery or block venous return. It is typically used following coronary angiography/ventriculography or percutaneous transluminal coronary angioplasty (PTCA). This is a single-use device.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Store in a dark, dry, cool place. Avoid extended exposure to light.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1 877 466 0109info@forgemedical.com

Regulatory Flags#

DUNS number
071018368
Device count
1
Lot or batch
true
Expiration date on label
true
No natural rubber latex
true

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
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00190776419127MillenniumAvalign Technologies, Inc.DXC2026-08-23
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00885403523277FOGARTY SOFTJAWBecton, Dickinson And CompanyDXC2026-07-30
10841156102012D-STATTELEFLEX INCORPORATEDDXC2026-07-30
00190776404178MillenniumAvalign Technologies, Inc.DXC2026-07-24
00190776404185MillenniumAvalign Technologies, Inc.DXC2026-07-24
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00810220800461Adler Instrument CompanyAdler, Inc.DXC2026-07-17
00190776397180MillenniumAvalign Technologies, Inc.DXC2026-07-16
00190776395605MillenniumAvalign Technologies, Inc.DXC2026-07-14
00190776395698MillenniumAvalign Technologies, Inc.DXC2026-07-14
00190776395711MillenniumAvalign Technologies, Inc.DXC2026-07-14
00192896123557Debakey Neonatal ClampSONTEC INSTRUMENTS, INC.DXC2026-07-10
00846159036152SCANLAN® Bulldog ClampSCANLAN INTERNATIONAL INCDXC2026-06-23
00846159036404SCANLAN® Bulldog ClampSCANLAN INTERNATIONAL INCDXC2026-06-09
00810220800348Adler Instrument CompanyAdler, Inc.DXC2026-06-02