FDA.reportPublic FDA data

Intercept Free

Primary DI
00150020014782
Brand
Intercept Free
Company
P H & S PRODUCTS LLC
Model
1LICFNG-3XL
Device description
Nitrile Two-Toned White/Green,Powder Free,Exam Grade Glove,Tested for use with Fentanyl,Heroin and Gastric Acid Size 3XL CTN
Published
2022-06-01
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
QDOFentanyl and other opioid protection glove

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
QDOFentanyl And Other Opioid Protection GloveGeneral Hospital1

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K220375000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K220375000Intercept Free, Nitrile Two Toned White/Green, Textured Fingertips, Powder-Free, Non-sterile, Ambidextrous, Beaded Cuff, Medical Examination Gloves, Tested for Use with Opioids Fentanyl citrate, Heroin, and both Opioids in simulated Gastric Acid (Vomit)Summit Glove, Inc.2022-04-13LZA

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00150020014782PackageGS1900In Commercial Distribution
00850020014781PrimaryGS10
00850020014798Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00150020014782001500200147821500200147820150020014782
00850020014781008500200147818500200147810850020014781
00850020014798008500200147988500200147980850020014798

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
+1(330)868-2239tcalkins@phs-products.com

Regulatory Flags#

DUNS number
968344643
Device count
90
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
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
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00850018123020ResQ-Grip79720PF-BKGR2020-08-01
00850018123044ResQ-Grip79730PF-BKGR2020-08-01
00850018123068ResQ-Grip79740PF-BKGR2020-08-01
00850018123082ResQ-Grip79750PF-BKGR2020-08-01
00850018123105ResQ-Grip79760PF-BKGR2020-08-01
00850018123129ResQ-Grip79770PF-BKGR2020-08-01
00850018123464Vital Shield SCFVSN7SC-S2020-08-01
00850018123488Vital Shield SCFVSN7SC-M2020-08-01
00850018123501Vital Shield SCFVSN7SC-L2020-08-01
00850018123525Vital Shield SCFVSN7SC-XL2020-08-01
00850018123549Vital Shield SCFVSN7SC-2XL2020-08-01
00850018123563Vital Shield SCFVSN7SC-3XL2020-08-01
00850018123587Flextreme1LFTNG-S2020-08-01
00850018123600Flextreme1LFTNG-M2020-08-01
00850018123624Flextreme1LFTNG-L2020-08-01
00850018123648Flextreme1LFTNG-XL2020-08-01
00850018123662Flextreme1LFTNG-2XL2020-08-01
00850018123686Flextreme1LFTNG-3XL2020-08-01
00850020014323ResQ-Grip79720PF-BKGR2020-08-01
00850020014347ResQ-Grip79730PF-BKGR2020-08-01

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