Syntervention

Primary DI
00850049994866
Brand
Syntervention
Company
ZIEN MEDICAL TECHNOLOGIES, INC.
Model
4008-203
Device description
"SWICKER is a sterile foam sponge designed for single-patient use. SWICKER is a highly absorbent sponge intended for use in a variety of surgical or medical procedures. SWICKER can be used in multiple surgical procedures and areas including patient prepping, open surgery, instrument padding, instrument cleaning, and wound care. SWICKER Radiopaque Sponge 2 Pack, 1.5"" x 3"" x .125"""
Published
2025-09-26
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
MR Safe
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
GDYGauze/Sponge, Internal, X-Ray Detectable

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GDYGauze/Sponge, Internal, X-Ray DetectableGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10850049994863PackageGS1100In Commercial Distribution
00850049994866PrimaryGS10
00850049993029Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1085004999486310850049994863
00850049994866008500499948668500499948660850049994866
00850049993029008500499930298500499930290850049993029

GMDN Terms#

Term, Definition table
TermDefinition
Radiopaque non-woven surgical spongeA non-medicated device made from a non-woven absorbent material (e.g., rayon/polyester) primarily intended to be used inside the body, on a surgical incision or applied to internal organs or structures to control bleeding, absorb fluid, or protect organs or structures from abrasion, drying, or contamination during a procedure; also referred to as a laparotomy sponge, it may also be used for prepping the patient. It is intended to produce less lint than woven gauze and contains an x-ray detectable marker [e.g., a thread or strand(s)] to help detect gossypiboma (sponge left inside patient). This is a single-use device.

Regulatory Flags#

DUNS number
017535668
Device count
2
Premarket exempt
true
Lot or batch
true
Expiration date on label
true

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