FDA.reportPublic FDA data

N-Dex

Primary DI
20038054686400
Brand
N-Dex
Company
SHOWA BEST GLOVE, INC.
Model
XL
Catalog number
M7005PFXL
Device description
Biodegradable Exam Use, powder-free, low-modulus 100%-nitrile, 9-1/2", 4-mil, rolled cuff, blue/Extra Large
Published
2023-02-20
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
LZAPolymer Patient Examination Glove

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LZAPolymer Patient Examination GloveGeneral Hospital1

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K211003000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K211003000SHOWA(R) Blue Nitrile Powder Free Medical Examination GloveShowa Best Glove, Inc.2022-01-19LZA

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
20038054686400PackageGS120In Commercial Distribution
00038054686406PrimaryGS10
10038054686403Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
2003805468640020038054686400
00038054686406000380546864060380546864060038054686406
1003805468640310038054686403

GMDN Terms#

Term, Definition table
TermDefinition
Nitrile examination/treatment glove, non-powdered, non-antimicrobialA device made of nitrile intended as a protective barrier when worn on the hands of healthcare providers during patient examination/treatment or for other sanitary purposes; its inner surface is not covered with powder and it does not include antimicrobial agents/materials. The device is used mainly as a two-way barrier to protect patient/staff against contaminants and risk of allergy to latex. It will have appropriate characteristics regarding tactility and comfort of use, and should provide appropriate physical properties (e.g., tensile strength, resistance to puncture, elasticity), and uniformity of dimensions (i.e., sizing consistency). This is a single-use device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
800-241-0323USA@Showagroup.com

Regulatory Flags#

DUNS number
807930412
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
true
Expiration date on label
false
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
00038054654306DermaThinXLM7002PFXL2023-03-31
00038054654313DermaThinXXLM7002PFXXL2023-03-31
00038054654375DermaThinSM7002PFS2023-03-31
00038054654382DermaThinMM7002PFM2023-03-31
00038054654399DermaThinLM7002PFL2023-03-31
10038054654303DermaThinXLM7002PFXL2023-03-31
10038054654310DermaThinXXLM7002PFXXL2023-03-31
00038054654368DermaThinXSM7002PFXS2023-03-31
10038054654372DermaThinSM7002PFS2023-03-31
10038054654389DermaThinMM7002PFM2023-03-31
10038054654396DermaThinLM7002PFL2023-03-31
00038054256104SHOWAXL5005PFXL2023-03-24
00038054256111SHOWAXXL5005PFXXL2023-03-24
00038054256166SHOWAXS5005PFXS2023-03-24
00038054256173SHOWAS5005PFS2023-03-24
00038054256180SHOWAM5005PFM2023-03-24
00038054256197SHOWAL5005PFL2023-03-24
10038054256101SHOWAXL5005PFXL2023-03-24
10038054256118SHOWAXXL5005PFXXL2023-03-24
10038054256163SHOWAXS5005PFXS2023-03-24

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