FDA.reportPublic FDA data

Alleset

Primary DI
06931918138681
Brand
Alleset
Company
GRI Medical & Electronic Technology Co., Ltd.
Model
Model 37-2120
Device description
Veress Needle_120mm_Non-Sterile_500ea/cs
Published
2021-04-22
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
HIFInsufflator, laparoscopic

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HIFInsufflator, LaparoscopicObstetrics/Gynecology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K172835000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K172835000GRI-Alleset Veress NeedleGri Medical and Electronic Technology Co., Ltd.2018-06-11HIF

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
16931918138688PrimaryGS10
06931918138681Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
1693191813868816931918138688
06931918138681069319181386816931918138681

GMDN Terms#

Term, Definition table
TermDefinition
General-purpose endoscopic needle, single-useA flexible, sterile, sharp bevel-edged, hollow tubular device intended to be manually-operated through a compatible endoscope to perform various needle functions (e.g., injection, aspiration, irrigation, puncture) during endoscopy. It is designed with appropriate shape, materials, gauge, and other characteristics (e.g., high-contrast tips) to function through the working channel of an endoscope. This is a single-use device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+86057383617385link_dong@gri-metc.com

Regulatory Flags#

DUNS number
679894738
Device count
500
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
false
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
16931918196756AllesetV91-6120-S12026-10-15
16942748412121AllesetV91-6122-S12026-10-15
16942748430514AllesetCP01020070CA01A2026-10-15
16942748480953AllesetV91-6132-S12026-10-15
16942748475843AllesetVM-CS0912026-09-08
16931918113425AllesetS90-35302026-09-29
16931918122397Alleset15-0700CW2026-09-29
16931918143040AllesetS90-3020-S22026-09-29
16931918143217AllesetS90-30202026-09-29
16931918143248Alleset90-8030-S12026-09-29
16931918153704AllesetS90-35202026-09-29
16931918155159AllesetS90-3030-S22026-09-29
16931918176680Alleset15-0500-C-HK2026-09-29
16931918182988AllesetS90-3530-S22026-09-29
16931918191614Alleset15-0952HK-WH2026-09-29
16931918192208AllesetV91-6130-S22026-09-29
16931918195544AllesetS90-3520-S22026-09-29
16931918198286AllesetS90-30302026-09-29
16931918199627Alleset80-09135G-S-CL2026-09-29
16931918100852Alleset80-08159-HB2026-07-28

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B3543000010ThoraClear Y ConnectorORANGE SURGICAL INSTRUMENTS, LLCHIF2025-11-25
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B354OSLPCDG51Lap-port closure device guides 5mm and 10/12 mmORANGE SURGICAL INSTRUMENTS, LLCHIF2024-03-07
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