Plastic needle MR safe, 2.0 mm diameter x 113 mm length, with mandrin

Primary DI
00810563022025
Brand
Plastic needle MR safe, 2.0 mm diameter x 113 mm length, with mandrin
Company
VARIAN MEDICAL SYSTEMS, INC.
Model
GM11014700
Catalog number
GM11014700
Published
2024-02-16
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
false

Product Codes#

Code, Name table
CodeName
JAQSystem, applicator, radionuclide, remote-controlled

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
JAQSystem, Applicator, Radionuclide, Remote-ControlledRadiology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K120341000
K141624000
K160815000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K120341000PLASTIC NEEDLE WITH MANDRIN 2.0 DIAMETER LENGTH 113MMVarian Medical Systems, Inc.2012-04-27JAQ
K141624000PLASTIC NEEDLE WITH MANDRIN, 2.0 MM DIAMETER, LENGTH, BLUNT TIP,PLASTIC NEEDLE WITH MANDRIN, 2.0 MM DIAMETER, LENGTH 113Varian Medical Systems, Inc.2015-03-10JAQ
K160815000Interstitial NeedlesVarian Medical Systems, Inc.2017-03-10JAQ

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10810563022022PackageGS110In Commercial Distribution
00810563022025PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1081056302202210810563022022
00810563022025008105630220258105630220250810563022025

GMDN Terms#

Term, Definition table
TermDefinition
Brachytherapy injection needleA sharp bevel-edged, hollow tubular metal instrument that is used to inject radionuclide into a body cavity or tissue as a source of nuclear radiation for cancer therapy (brachytherapy). The device may be pre-sterilized and preloaded, and may have a tip enhanced for ultrasound-guided implantation. This is a single-use device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
009120817
Device count
1
DM exempt
true
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

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