FDA.reportPublic FDA data

Acu-Punch

Primary DI
00814105020944
Brand
Acu-Punch
Company
ACUDERM, INC.
Model
P4
Device description
Acu-Punch, 4mm, Single
Published
2020-09-22
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
EMEPunch, Biopsy, Surgical

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
EMEPunch, Biopsy, SurgicalDental1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00814105021484PackageGS110In Commercial Distribution
10814105020941PackageGS125In Commercial Distribution
10814105021535PackageGS120In Commercial Distribution
10814105021573PackageGS120In Commercial Distribution
10814105021610PackageGS120In Commercial Distribution
20814105020948PackageGS150In Commercial Distribution
00814105020944PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00814105021484008141050214848141050214840814105021484
1081410502094110814105020941
1081410502153510814105021535
1081410502157310814105021573
1081410502161010814105021610
2081410502094820814105020948
00814105020944008141050209448141050209440814105020944

GMDN Terms#

Term, Definition table
TermDefinition
Skin-coring punch, single-useA hand-held manual surgical instrument designed to cut out (core) sections of skin as part of a dermatological procedure to remove skin lesions or to obtain skin-tissue specimens. It consists of a handle and a cylindrical distal tip which has a bevelled, sharp cutting edge, which when pressed into the skin surface and gently rotated will penetrate and cut through the skin allowing that section to be removed. It is typically made of high-grade stainless steel and is available in various cutting head sizes; it is not a biopsy gun. This is a single-use device.

Regulatory Flags#

DUNS number
071426803
Device count
1
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
00814105020005Acu-Dispo-CuretteR012020-09-22
00814105020012Acu-Dispo-CuretteR022020-09-22
00814105020029Acu-Dispo-CuretteR032020-09-22
00814105020036Acu-Dispo-CuretteR042020-09-22
00814105020043Acu-Dispo-CuretteR052020-09-22
00814105020050Acu-Dispo-CuretteR072020-09-22
00814105020883Acu-PunchP12020-09-22
00814105020890Acu-PunchP1.52020-09-22
00814105020906Acu-PunchP22020-09-22
00814105020913Acu-PunchP2.52020-09-22
00814105020920Acu-PunchP32020-09-22
00814105020937Acu-PunchP3.52020-09-22
00814105020951Acu-PunchP4.52020-09-22
00814105020968Acu-PunchP52020-09-22
00814105020975Acu-PunchP62020-09-22
00814105020982Acu-PunchP72020-09-22
00814105020999Acu-PunchP82020-09-22
00814105021002Acu-PunchP102020-09-22
00814105021019Acu-PunchP122020-09-22
00814105021316Acu-Dispo-CuretteRCOM2020-09-22

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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