DynaLube, Sterile, 2 oz. Tube

GUDID 00616784125213

DYNAREX CORPORATION

General-body orifice lubricant, sterile General-body orifice lubricant, sterile General-body orifice lubricant, sterile General-body orifice lubricant, sterile General-body orifice lubricant, sterile General-body orifice lubricant, sterile General-body orifice lubricant General-body orifice lubricant General-body orifice lubricant General-body orifice lubricant General-body orifice lubricant General-body orifice lubricant General-body orifice lubricant General-body orifice lubricant General-body orifice lubricant General-body orifice lubricant General-body orifice lubricant
Primary Device ID00616784125213
NIH Device Record Keyd89844a2-425d-433b-a874-9fa0128c63e8
Commercial Distribution StatusIn Commercial Distribution
Brand NameDynaLube, Sterile, 2 oz. Tube
Version Model Number1252
Company DUNS008124539
Company NameDYNAREX CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100616784125213 [Primary]
GS100616784125220 [Package]
Package: Box [12 Units]
In Commercial Distribution
GS100616784125237 [Package]
Contains: 00616784125220
Package: Case [6 Units]
In Commercial Distribution

FDA Product Code

KMJLubricant, Patient

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-05-31
Device Publish Date2022-05-23

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00840117333024 - XeroBurn Sterile Burn Dressing Blanket 60"x 70"2024-04-02 60"x 70"
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