FDA.reportPublic FDA data

Globe

Primary DI
00850026393033
Brand
Globe
Company
Trifecta Pharmaceuticals USA LLC
Model
20206
Device description
Globe Non-Adherent Pads 3 x 8 Box of 50
Published
2021-02-28
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
NABGauze / Sponge,Nonresorbable For External Use

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
NABGauze / Sponge,Nonresorbable For External UseGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00850026393071PrimaryGS10
00850026393033Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00850026393071008500263930718500263930710850026393071
00850026393033008500263930338500263930330850026393033

GMDN Terms#

Term, Definition table
TermDefinition
Wound-nonadherent dressing, absorbent, antimicrobialA wound covering typically in the form of a multi-layered pad having a material on its skin-contact surface that prevents adherence to the wound bed (e.g., soft silicone), thereby decreasing the potential for wound trauma, and that contains an antimicrobial agent [e.g., silver (Ag), honey]. It is used to absorb blood and exudates from the wound, while protecting the wound from external contamination and maintaining a moist internal environment. It may be used as a primary or secondary dressing with other wound-care products to treat chronic and postoperative wounds, burns, ulcers, abrasions, cuts, or puncture sites. This is a single-use device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
888-296-9067info@trifecta-pharma.com

Regulatory Flags#

DUNS number
079424163
Device count
50
DM exempt
false
Premarket exempt
true
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
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00850026393064Globe 202022021-02-28
00850026393118Globe 202092021-02-28
00850026393071Globe 202062021-02-28
00850026393088Globe 202072021-02-28
00850026393095Globe 202082021-02-28
00850026393019Globe 202022021-02-28
00850026393040Globe 202072021-02-28
00850026393026Globe 202082021-02-28
00850026393002Globe 202092021-02-28

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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