CODMAN BICOL 801460

GUDID 20886704036668

CODMAN BICOL Collagen Sponge

CODMAN & SHURTLEFF, INC.

Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge Neurosurgical sponge
Primary Device ID20886704036668
NIH Device Record Key5301d14b-9f42-4a58-8250-fb24121d3675
Commercial Distribution Discontinuation2022-09-01
Commercial Distribution StatusIn Commercial Distribution
Brand NameCODMAN BICOL
Version Model Number80-1460
Catalog Number801460
Company DUNS607846297
Company NameCODMAN & SHURTLEFF, 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

Customer Support Contacts

Phone+1(800)255-2500
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Device Identifiers

Device Issuing AgencyDevice ID
GS110886704036661 [Primary]
GS120886704036668 [Package]
Contains: 10886704036661
Package: Carton [10 Units]
Discontinued: 2022-09-01
In Commercial Distribution

FDA Product Code

GELGAUZE/SPONGE, INTERNAL, WITH DRUG/BIOLOGIC, ANIMAL SOURCE MATERIAL
HBANeurosurgical paddie

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2021-10-14
Device Publish Date2016-06-30

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10886704085355 - CEREGLIDE2023-07-17 CEREGLIDE 71 Intermediate Catheter 115 cm 0.071 in (1.80 mm) 0.0820 in (2.08 mm) 0.0825 in (2.10 mm)
10886704085386 - CEREGLIDE2023-07-17 CEREGLIDE 71 Intermediate Catheter 137 cm 0.071 in (1.80 mm) 0.0820 in (2.08 mm) 0.0825 in (2.10 mm)
10886704085409 - CEREGLIDE2023-07-17 CEREGLIDE 71 Intermediate Catheter 132 cm 0.071 in (1.80 mm) 0.0820 in (2.08 mm) 0.0825 in (2.10 mm)
10886704085423 - CEREGLIDE2023-07-17 CEREGLIDE 71 Intermediate Catheter 125 cm 0.071 in (1.80 mm) 0.0820 in (2.08 mm) 0.0825 in (2.10 mm)
10886704078630 - CODMAN MALIS CMC2023-04-04 CODMAN MALIS CMC-V Generator
10886704046912 - CODMAN HAKIM RICKHAM2022-10-10 CODMAN HAKIM Precision Fixed Pressure Valve MICRO II With Large RICKHAM Reservoir Operating Pressure: 100mm H2O Plus or Minus 10
10886704045366 - CODMAN HAKIM SIPHONGUARD2022-09-01 CODMAN HAKIM Precision Fixed Pressure Valve with SIPHONGUARD Device Operating Pressure: 130mm H2O High Range Includes: Ventricul
10886704015505 - CRANIOPLASTIC2022-03-01 Codman CRANIOPLASTIC Resinous Material for Repairing Cranial Defects
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