FDA.reportPublic FDA data

NUSA

Primary DI
00810007662411
Brand
NUSA
Company
HOURGLASS INTERNATIONAL INC
Model
203
Device description
PF Nitrile Exam Gloves - L, 200/BX, Made In USA, Tested For Use With Chemotherapy Drugs and Fentanyl
Published
2026-01-01
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
LZAPolymer Patient Examination Glove

Product Code Classifications#

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

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K233970000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K233970000Nephron Nitrile™, Nitrile Powder-Free Examination Blue Gloves (Tested For Use With Chemotherapy Drugs and Fentanyl)Nephron Nitrile, LLC2024-01-16LZA

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00810007662411PackageGS110In Commercial Distribution
00810007662367PrimaryGS10
00810007662312Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810007662411008100076624118100076624110810007662411
00810007662367008100076623678100076623670810007662367
00810007662312008100076623128100076623120810007662312

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.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Special Storage Condition, Specify: Store under cool dry conditions. Avoid direct sunlight. Open box should be shielded from direct sunlight or fluorescent lighting.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
800-277-0994request@hourglass-intl.com

Regulatory Flags#

DUNS number
026777252
Device count
200
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
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
00810007662336NUSA2002026-01-01
00810007662343NUSA2012026-01-01
00810007662350NUSA2022026-01-01
00810007662367NUSA2032026-01-01
00810007662374NUSA2042026-01-01
00810007662381NUSA2002026-01-01
00810007662398NUSA2012026-01-01
00810007662404NUSA2022026-01-01
00810007662428NUSA2042026-01-01
00810007662480HANDPRO55002025-12-15
00810007662497HANDPRO55012025-12-15
00810007662503HANDPRO55022025-12-15
00810007662510HANDPRO55032025-12-15
00810007662527HANDPRO55042025-12-15
00810007662596HANDPRO55052025-12-15
00810007662534HANDPRO55002025-12-15
00810007662541HANDPRO55012025-12-15
00810007662558HANDPRO55022025-12-15
00810007662565HANDPRO55032025-12-15
00810007662572HANDPRO55042025-12-15

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