PERL R10

GUDID 15420045514072

Hologic, Inc.

Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use
Primary Device ID15420045514072
NIH Device Record Keyfb2d2787-450d-425a-800b-1f257b8d1c6e
Commercial Distribution StatusIn Commercial Distribution
Brand NamePERL
Version Model NumberR10
Catalog NumberR10
Company DUNS018925968
Company NameHologic, Inc.
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS115420045514072 [Primary]

FDA Product Code

GDFGUIDE, NEEDLE, SURGICAL

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-09-27
Device Publish Date2021-09-17

On-Brand Devices [PERL]

25420045514079R10-5
15420045514096R20
15420045514089R15
15420045514072R10

Trademark Results [PERL]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PERL
PERL
88812820 not registered Live/Pending
Don Polly, LLC
2020-02-27
PERL
PERL
87333160 not registered Dead/Abandoned
DoseLogix, LLC
2017-02-13
PERL
PERL
86799744 5291652 Live/Registered
Focal Therapeutics, Inc.
2015-10-26
PERL
PERL
85767741 not registered Dead/Abandoned
COOPER TECHNOLOGIES COMPANY
2012-10-31
PERL
PERL
78340172 not registered Dead/Abandoned
PERL, LLC
2003-12-12
PERL
PERL
76629502 3178940 Live/Registered
Yet Another Society
2005-01-27
PERL
PERL
75846028 2389965 Dead/Cancelled
PERL, INC.
1999-11-10
PERL
PERL
73768035 not registered Dead/Abandoned
PERL BRAND FOODS CORPORATION
1988-12-08
PERL
PERL
73768034 not registered Dead/Abandoned
PERL BRAND FOODS CORPORATION
1988-12-08
PERL
PERL
73135754 1099919 Dead/Expired
PERL, INC.
1977-07-28
PERL
PERL
71678095 0622762 Dead/Expired
DELITE PRODUCTS COMPANY
1954-12-10
PERL
PERL
71336521 0305915 Dead/Expired
NAAMLOOZE VENNOOTSCHAP HERO CONSERVEN BREDA
1933-04-06

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