EARP Retractor

GUDID 00810135960762

EARP Retractor, EARP RETRACTOR CONNECTOR. The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with nerve retraction, to increase working corridor and improve line of sight to working area.

NVISION BIOMEDICAL TECHNOLOGIES, INC.

Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable
Primary Device ID00810135960762
NIH Device Record Key12a34645-5707-412a-a54d-7fbbdfbf859e
Commercial Distribution StatusIn Commercial Distribution
Brand NameEARP Retractor
Version Model NumberEARP-R_003
Company DUNS047486041
Company NameNVISION BIOMEDICAL TECHNOLOGIES, 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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com
Phone210-598-5641
Emaildiana@nvisionbiomed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100810135960762 [Primary]

FDA Product Code

GADRetractor

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

[00810135960762]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-10-06
Device Publish Date2023-09-28

On-Brand Devices [EARP Retractor]

00810135960762EARP Retractor, EARP RETRACTOR CONNECTOR. The EARP Retractor is used in conjunction with TeDan P
00810135960755EARP Retractor, EARP CRADLE ASSEMBLY. The EARP Retractor is used in conjunction with TeDan Phant
00810135960748EARP Retractor, EARP BLADE 150. The EARP Retractor is used in conjunction with TeDan Phantom M
00810135960731EARP Retractor, EARP BLADE 140. The EARP Retractor is used in conjunction with TeDan Phantom M
00810135960724EARP Retractor, EARP BLADE 130. The EARP Retractor is used in conjunction with TeDan Phantom M
00810135960717EARP Retractor, EARP BLADE 120. The EARP Retractor is used in conjunction with TeDan Phantom M
00810135960700EARP Retractor, EARP BLADE 110. The EARP Retractor is used in conjunction with TeDan Phantom M
00810135960694EARP Retractor, EARP BLADE 100 The EARP Retractor is used in conjunction with TeDan Phantom ML M
00810135960687EARP Retractor, EARP BLADE 90. The EARP Retractor is used in conjunction with TeDan Phantom ML
00810135960670EARP Retractor, EARP BLADE 80. The EARP Retractor is used in conjunction with TeDan Phantom ML
00810135960663EARP Retractor, EARP BLADE 70. The EARP Retractor is used in conjunction with TeDan Phantom ML
00810135960656EARP Retractor, EARP BLADE 60. The EARP Retractor is used in conjunction with TeDan Phantom ML
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