Cypris ARC

GUDID 00854037007002

Cypris Medical, Inc.

Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use Suturing unit, single-use
Primary Device ID00854037007002
NIH Device Record Key6eb77c11-e860-473f-bfed-2f8e4666f5c6
Commercial Distribution StatusIn Commercial Distribution
Brand NameCypris ARC
Version Model NumberCM3050
Company DUNS117322746
Company NameCypris Medical, Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
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 Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100854037007002 [Primary]

FDA Product Code

GEJCarrier, Ligature

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-08-18
Device Publish Date2022-08-10

Devices Manufactured by Cypris Medical, Inc.

00854037007170 - eXact Suture Placement Device2024-06-18
00854037007026 - eXact Suture 4-0 PP2024-04-10 eXact Suture, 4-0 Polypropylene
00854037007040 - eXact Suture 3-0 PP2024-04-10 eXact Suture, 3-0 Polypropylene
00854037007064 - eXact Suture 2-0 PTFE2024-04-10 eXact Suture, 2-0 PTFE
00854037007088 - eXact Suture 3-0 PTFE2024-04-10 eXact Suture, 3-0 PTFE
00854037007101 - eXact Suture 4-0 PDO2024-04-10 eXact Suture, 4-0 PDO
00854037007125 - eXact Suture 3-0 PDO2024-04-10 eXact Suture, 3-0 PDO
00854037007149 - eXact 5.12023-03-08

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