Acumatch A Series 132-32-07

GUDID 10885862023209

Exactech, Inc.

Non-constrained polyethylene acetabular liner
Primary Device ID10885862023209
NIH Device Record Key9cf513e6-37f8-44e0-ad57-55730400f098
Commercial Distribution Discontinuation2024-06-13
Commercial Distribution StatusNot in Commercial Distribution
Brand NameAcumatch A Series
Version Model Number132-32-07
Catalog Number132-32-07
Company DUNS157565946
Company NameExactech, Inc.
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 Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Lumen/Inner Diameter32 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Lumen/Inner Diameter32 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Lumen/Inner Diameter32 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Lumen/Inner Diameter32 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Lumen/Inner Diameter32 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Lumen/Inner Diameter32 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Lumen/Inner Diameter32 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Lumen/Inner Diameter32 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Lumen/Inner Diameter32 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Lumen/Inner Diameter32 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Lumen/Inner Diameter32 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Lumen/Inner Diameter32 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS110885862023209 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LPHProsthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2025-08-29
Device Publish Date2015-08-10

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10885862021045122-01-58
10885862021038122-01-56
10885862021021122-01-54
10885862021014122-01-52
10885862021007122-01-50
10885862020994122-01-48
10885862020987122-01-46
10885862020970122-01-44
10885862019820120-01-70
10885862019813120-01-68
10885862019806120-01-66
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