FDA.report

N/A

Primary DI
00841036045913
Brand
N/A
Company
BIOMET MICROFIXATION, INC
Model
39-0011
Catalog number
39-0011
Published
2018-09-07
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Related Records

Contact Domains

Product Codes

CodeName
KYWCONTAINER, LIQUID MEDICATION, GRADUATED

Product Code Classifications

CodeDeviceSpecialtyClass
KYWContainer, Liquid Medication, GraduatedGeneral Hospital1

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00841036045913PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
00841036045913008410360459138410360459130841036045913

GMDN Terms

TermDefinition
Forceps jarA tall, slender, cylindrical vessel designed for holding various types of forceps prior to and during a surgical intervention or an examination in an operating room (OR) or examination room. It is typically made of high-grade stainless steel or sterilizable plastic material (e.g., polypropylene) and will have a wide or weighted base to give it stability. It may have a hinged lid with a semicircular notch in its forward edge so that the handles of the forceps can protrude. The jar may hold a disinfecting solution while in use. This is a reusable device.

Sterilization Methods

Method
Moist Heat or Steam Sterilization

Contacts

PhoneEmail
+1(904)741-4400FXJAX-ORDERS@ZIMMERBIOMET.COM

Regulatory Flags

DUNS number
046189866
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
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
true

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