FDA.reportPublic FDA data

GLIDEWIRE

Primary DI
34987350755934
Brand
GLIDEWIRE
Company
TERUMO CORPORATION
Model
UWSS5125
Catalog number
RF*PS25153U
Device description
RADIFOCUS GLIDEWIRE
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
true
Single use
true

Product Codes#

Code, Name table
CodeName
KODCATHETER, UROLOGICAL

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KODCatheter, UrologicalGastroenterology, Urology2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
34987350755934PackageGS15In Commercial Distribution
54987350755938PackageGS15In Commercial Distribution
04987350755933PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
3498735075593434987350755934
5498735075593854987350755938
04987350755933049873507559334987350755933

GMDN Terms#

Term, Definition table
TermDefinition
General-purpose non-vascular guidewireA non-dedicated metal wire designed to position a catheter or similar interventional device (e.g., a dilator or an endoscope) within a lumen of the gastrointestinal (GI) tract, the tracheobronchial tree, and the urinary tract (i.e., not dedicated to either clinical application). Typically, the catheter is advanced over the wire after the wire has been manoeuvred to a treatment site (e.g., site of stent-placement). It is available in a variety of diameters and lengths, may have fluoroscopic markers, or be fitted with an introducer for entering the working channel of the catheter or other interventional device. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0
Length150Centimeter
Outer Diameter0.64Millimeter

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Fragile.Keep away from rain. Keep away from sunlight.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)283-7866tmccustomer.admin@terumomedica

Regulatory Flags#

DUNS number
690543319
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
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
04987350740601GLIDEWIRE GT-RGT*GW1618AGT*GW1618A2026-02-06
04987350740625GLIDEWIRE GT-RGT*GA1818AGT*GA1818A2026-02-06
04987350740649GLIDEWIRE GT-RGT*GA1822AGT*GA1822A2026-02-06
54987350740668GLIDEWIRE GT-RGT*GE1818AGT*GE1818A2026-02-06
04987350740687GLIDEWIRE GT-RGT*GE1822AGT*GE1822A2026-02-06
54987350740699GLIDEWIRE GT-RGT*GW1818AGT*GW1818A2026-02-06
04987350740700GLIDEWIRE GT-RGT*GW1822AGT*GW1822A2026-02-06
04987350745422GLIDEWIRE GT-RGT*GW1622AGT*GW1622A2026-02-06
04987350744487DUALVIEWTU-DSS01CTU*DV01U2026-01-21
54953170465050VISIGLIDEG-240-2527AN36222312025-07-14
54953170465067VISIGLIDEG-240-2545AN36224312025-07-14
54953170465074VISIGLIDEG-240-3527AN36226312025-07-14
54953170465081VISIGLIDEG-240-3545AN36228312025-07-14
54953170465098VISIGLIDEG-240-2527SN36221312025-07-14
54953170465104VISIGLIDEG-240-2545SN36223312025-07-14
54953170465111VISIGLIDEG-240-3527SN36225312025-07-14
54953170465128VISIGLIDEG-240-3545SN36227312025-07-14
54953170465135VISIGLIDE2G-260-2527AN53677312025-07-14
54953170465142VISIGLIDE2G-260-2545AN53681312025-07-14
54953170465159VISIGLIDE2G-260-3527AN53679312025-07-14

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
24026704942057RUSCHTELEFLEX INCORPORATEDKOD2026-03-23
04026704942060RUSCHTELEFLEX INCORPORATEDKOD2026-03-23
04026704942077RUSCHTELEFLEX INCORPORATEDKOD2026-03-23
24026704942088RUSCHTELEFLEX INCORPORATEDKOD2026-03-23
24026704942095RUSCHTELEFLEX INCORPORATEDKOD2026-03-23
24026704942101RUSCHTELEFLEX INCORPORATEDKOD2026-03-23
04026704942114RUSCHTELEFLEX INCORPORATEDKOD2026-03-23
24026704942125RUSCHTELEFLEX INCORPORATEDKOD2026-03-23
04026704942138RUSCHTELEFLEX INCORPORATEDKOD2026-03-23
24026704942149RUSCHTELEFLEX INCORPORATEDKOD2026-03-23
04026704942152RUSCHTELEFLEX INCORPORATEDKOD2026-03-23
24026704942163RUSCHTELEFLEX INCORPORATEDKOD2026-03-23
24026704942170RUSCHTELEFLEX INCORPORATEDKOD2026-03-23
04026704942183RUSCHTELEFLEX INCORPORATEDKOD2026-03-23
20192253024255DoverCardinal Health 200, LLCKOD2026-03-20
50192253024263DoverCardinal Health 200, LLCKOD2026-03-20
50192253024270DoverCardinal Health 200, LLCKOD2026-03-20
50192253024300DoverCardinal Health 200, LLCKOD2026-03-20
20885380202596DoverCardinal Health 200, LLCKOD2026-03-20
50850058254673EZ-Advancer®HR PHARMACEUTICALS INC.KOD2026-03-06
04026704937158RUSCHTELEFLEX INCORPORATEDKOD2026-02-27
34026704937166RUSCHTELEFLEX INCORPORATEDKOD2026-02-27
04026704937172RUSCHTELEFLEX INCORPORATEDKOD2026-02-27
34026704937180RUSCHTELEFLEX INCORPORATEDKOD2026-02-27
04026704937196RUSCHTELEFLEX INCORPORATEDKOD2026-02-27
34026704937203RUSCHTELEFLEX INCORPORATEDKOD2026-02-27
20854913006185Urinary Catheter, 16 FrUROGEN PHARMA LTDKOD2025-11-17
20854913006192Urinary Catheter, 16 FrUROGEN PHARMA LTDKOD2025-11-17
20854913006154Urinary Catheter, 16 FrUROGEN PHARMA LTDKOD2025-11-16
20854913006161Urinary Catheter, 16 FrUROGEN PHARMA LTDKOD2025-11-16