FDA.reportPublic FDA data

LiteTouch

Primary DI
30732671305320
Brand
LiteTouch
Company
AMITY HOLDINGS, LLC
Model
532
Device description
MediCore's "LiteTouch" Brand Insulin Pen Needle
Published
2016-09-01
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
FMINeedle, Hypodermic, Single Lumen

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FMINeedle, Hypodermic, Single LumenGeneral Hospital2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
20732671205326PackageGS112Not in Commercial Distribution
30732671305320PackageGS14Not in Commercial Distribution
10732671105322PrimaryGS10
00732671005328Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
2073267120532620732671205326
3073267130532030732671305320
1073267110532210732671105322
00732671005328007326710053287326710053280732671005328

GMDN Terms#

Term, Definition table
TermDefinition
Autoinjector needleA device designed for the parenteral administration of a drug contained in a cartridge that forms part of, is attached to, or inserted into an autoinjector (drug pen injector). It is used by persons requiring regular, self-administrated dosages of insulin, hormones, or other pharmaceuticals. This device will typically be constructed as a double-ended, stainless steel needle of various sizes that is fixed to a threaded hub of plastic to which the drug pen injector is connected. This device is packaged in a sealed sterility barrier, and might include needle shielding safety features to reduce the risk of needle stick injury. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Length5Millimeter
Needle Gauge31Gauge

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
800 327 8894wconety@medicore.com

Regulatory Flags#

DUNS number
016069284
Device count
100
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
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00732671009319PIP9319312019-12-30
00732671009326PIP9329322019-12-30
00732671009418Pip9419412021-06-21
10732671209426Pip9429422021-06-21
00732671109422Pip 942-2942-22021-06-21
30732671309403Pip940-50940-502026-04-16
00732671009401Pip9409402021-06-21
00732671009425Pip 942-1942-12021-06-21
10732671109023Pip9029022020-08-27
10732671109030PIP9039032020-08-27
10732671105315LiteTouch5312016-09-01
10732671105322LiteTouch5322016-09-01
10732671105339LiteTouch5332016-09-01
10732671105346LiteTouch5342016-09-01
10732671105353LiteTouch5352016-09-01
10732671106176LiteTouch6172016-09-01
10732671106183LiteTouch6182016-09-01
00732671021182LiteTouch211821182021-12-21
00732671022110LiteTouch 221122112021-06-21
00732671022127LiteTouch221222122021-06-21

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