DERMATOUCH

Primary DI
00810169802502
Brand
DERMATOUCH
Company
PRIME SOLUTIONS, INC.
Model
81950MD/M
Published
2025-12-19
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Single use
true

Product Codes#

Code, Name table
CodeName
LYZVinyl Patient Examination Glove

Product Code Classifications#

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

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K170735000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K170735000Powder-Free Clear Vinyl Patient Examination GlovesZibo Yue Fan Medical Products Co, Ltd.2017-06-27LYZ

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00810169802533PackageGS110In Commercial Distribution
00810169802502PrimaryGS10
10810169802509Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810169802533008101698025338101698025330810169802533
00810169802502008101698025028101698025020810169802502
1081016980250910810169802509

GMDN Terms#

Term, Definition table
TermDefinition
Vinyl examination/treatment glove, non-powderedA non-sterile device made of vinyl 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 talcum powder and it does not have antimicrobial features. 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.

Regulatory Flags#

DUNS number
093300590
Device count
100

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00810169802373DERMATOUCH82235MD/XS2026-04-24
00810169802380DERMATOUCH82235MD/S2026-04-24
00810169802397DERMATOUCH82235MD/M2026-04-24
00810169802403DERMATOUCH82235MD/L2026-04-24
00810169802410DERMATOUCH82235MD/XL2026-04-24
00810169802427DERMATOUCH82235MD/XXL2026-04-24
00810169802199DERMATOUCH81260MD/S2026-02-10
00810169802205DERMATOUCH81260MD/M2026-02-10
00810169802212DERMATOUCH81260MD/L2026-02-10
00810169802229DERMATOUCH81260MD/XL2026-02-10
00810169802236DERMATOUCH81260MD/2XL2026-02-10
00810169802243DERMATOUCH81260MD/S2026-02-10
00810169802250DERMATOUCH81260MD/M2026-02-10
00810169802267DERMATOUCH81260MD/L2026-02-10
00810169802274DERMATOUCH81260MD/XL2026-02-10
00810169802281DERMATOUCH81260MD/2XL2026-02-10
00810169800911DERMATOUCH81150MD/S2025-12-30
00810169800928DERMATOUCH81150MD/M2025-12-30
00810169800935DERMATOUCH81150MD/L2025-12-30
00810169800942DERMATOUCH81150MD/XL2025-12-30

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