WECK VISTA

Primary DI
10886874112523
Brand
WECK VISTA
Company
INTUITIVE SURGICAL, INC.
Model
470359
Device description
BLADELESS OBTURATOR
Published
2016-07-08
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
GCJLaparoscope, general & plastic surgery

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GCJLaparoscope, General & Plastic SurgeryGastroenterology, Urology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K152663000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K152663000Bladeless Optical ObturatorsIntuitive Surgical, Inc.2015-10-16GCJ

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10886874112523PackageGS16In Commercial Distribution
30886874112527PackageGS15In Commercial Distribution
00886874112526PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1088687411252310886874112523
3088687411252730886874112527
00886874112526008868741125268868741125260886874112526

GMDN Terms#

Term, Definition table
TermDefinition
Laparoscopic trocar blade, single-useA sterile, rigid, surgical instrument with a sharp pyramidal or conical point intended to puncture the abdominal wall to facilitate the introduction of a separate laparoscopic access cannula (not included) during laparoscopy. It is intended to fill the lumen of the laparoscopic access cannula, whereby following puncture it is withdrawn to provide a single-lumen access port to the abdominal cavity. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Outer Diameter8Millimeter

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
938647021
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
00886874114384EndoWrist SP4300602018-09-20
00886874110720daVinci Xi3806522016-07-08
00886874116272PlanPoint3807182019-03-21
10886874114343None4300122018-09-20
00886874113509EntryGuide4300222018-09-20
00886874114353None4300202018-09-20
00886874114377None4300352018-09-20
00886874119549None4300732021-03-11
00886874119556None4300752021-03-11
00886874121726Sureform4885302022-05-11
00886874121917Sureform48230B2022-05-11
00886874121924Sureform48230W2022-05-11
00886874121931Sureform48230M2022-05-11
00886874123645SureForm4365022025-06-20
00886874123652SureForm4365042025-06-20
00886874124598None4327012025-07-08
00886874125618Force Feedback4770062026-03-26
00886874125625Force Feedback4770492026-03-26
00886874125632Force Feedback4770932026-03-26
00886874125649Force Feedback4771722026-03-26

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Primary DI, Brand, Company table
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00198506092848ELMED INCORPORATEDELMED INCORPORATEDGCJ2026-07-22
00198506092862ELMED INCORPORATEDELMED INCORPORATEDGCJ2026-07-22
14026704645333WECKTELEFLEX INCORPORATEDGCJ2026-07-21
00198506092176ELMED INCORPORATEDELMED INCORPORATEDGCJ2026-07-17
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B382SD90781001000Surgical DirectSurgical Direct, Inc.GCJ2026-07-17
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B382SD1184590Surgical DirectSurgical Direct, Inc.GCJ2026-07-14
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B382SD7751586C0Surgical DirectSurgical Direct, Inc.GCJ2026-07-14
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00850045863012ArthroFree® 2 ReceiverLazurite Holdings LLCGCJ2026-07-10
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B382SD883110450Surgical DirectSurgical Direct, Inc.GCJ2026-07-10
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00190776421731MillenniumAvalign Technologies, Inc.GCJ2026-06-24
00190776421663MillenniumAvalign Technologies, Inc.GCJ2026-06-23