Oasis

GUDID B031DR60801

Sterile Surgical Drapes 60"X80"

American Health Service Sales Corporation

Patient surgical drape, single-use, sterile
Primary Device IDB031DR60801
NIH Device Record Key0e2391b7-1f92-479f-af5f-a869946bde6f
Commercial Distribution StatusIn Commercial Distribution
Brand NameOasis
Version Model NumberDR6080
Company DUNS556115970
Company NameAmerican Health Service Sales Corporation
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 Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB031DR60800 [Primary]
HIBCCB031DR60801 [Package]
Contains: B031DR60800
Package: Box [75 Units]
In Commercial Distribution

FDA Product Code

KKXDrape, Surgical

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-10-08
Device Publish Date2019-09-30

On-Brand Devices [Oasis]

B031TPORTMB0IV T-Connector 6" Microbore .
B031TPORT1IV T-Connector 6" Standard Bore.
B031SHARP4G1SHARPS CONTAINER, 4 GALLON
B031SHARP2G1SHARPS CONTAINER, 2 GALLON
B031SHARP1Q1SHARPS CONTAINER, 1 QT
B031SHARP1G1SHARPS CONTAINER, 1 GALLON
B031MVZ5870SUTURE,PDO,0,NFSL
B031MVZ4680SUTURE,PDO,1,NCP-1
B031MVZ4670SUTURE,PDO,0,NCP-1
B031MVZ4660SUTURE,PDO,2-0,NCP-1
B031MVZ4520SUTURE,PDO,3-0,NFS-1
B031MVZ4510SUTURE,PDO,2-0,NFS-1
B031MVZ3980SUTURE,PDO,3-0,NFS-2
B031MVZ3970SUTURE,PDO,4-0,NFS-2
B031MVZ3410SUTURE,PDO,1,NCT-1
B031MVZ3400SUTURE,PDO,0,NCT-1
B031MVZ3390SUTURE,PDO,2-0,NCT-1
B031MVZ3340SUTURE,PDO,0,NCT-2
B031MVZ3330SUTURE,PDO,2-0,NCT-2
B031MVZ3320SUTURE,PDO,3-0,NCT-2
B031MVZ3170SUTURE,PDO, 2-0, NSH
B031MVZ3160SUTURE,PDO,3-0,NSH
B031MVZ3151SUTURE,PDO,4-0,NSH
B031MVZ3110SUTURE,PDO,3-0,NSH-1
B031MVZ3100SUTURE,PDO,4-0,NSH-1
B031MVY9870SUTURE, MONOFYL, 0, NFSL
B031MVY9670SUTURE, MONOFYL, 0, NCP-1
B031MVY9430SUTURE, MONOFYL, 2-0, NFS-1
B031MVY9420SUTURE, MONOFYL, 3-0, NFS-1
B031MVY9230SUTURE, MONOFYL, 3-0, NFS-2
B031MVY9220SUTURE, MONOFYL, 4-0, NFS-2
B031MVY3460SUTURE, MONOFYL, 0, NCT-1
B031MVY3450SUTURE, MONOFYL, 2-0, NCT-1
B031MVY3440SUTURE, MONOFYL, 3-0, NCT-1
B031MVN6660SUTURE,NYLON,1,NFSL
B031MVN6650SUTURE,NYLON,0,NFSL
B031MVJ5870SUTURE,PGA,0,NFSL
B031MVJ4680SUTURE,PGA,1,NCP-1
B031MVJ4670SUTURE,PGA,0,NCP-1
B031MVJ4660SUTURE,PGA,2-0,NCP-1
B031MVJ4610SUTURE,PGA,2-0,NX-1
B031MVJ4600SUTURE,PGA,3-0,NX-1
B031MVJ4530SUTURE,PGA,2-0,NFS-1
B031MVJ4520SUTURE,PGA,3-0,NFS-1
B031MVJ4510SUTURE,PGA,4-0,NFS-1
B031MVJ3980SUTURE,PGA,3-0,NFS-2
B031MVJ3970SUTURE,PGA,4-0,NFS-2
B031MVJ3410SUTURE,PGA,1,NCT-1
B031MVJ3400SUTURE,PGA,0,NCT-1
B031MVJ3390SUTURE,PGA,2-0,NCT-1

Trademark Results [Oasis]

Mark Image

Registration | Serial
Company
Trademark
Application Date
OASIS
OASIS
98762169 not registered Live/Pending
Wind Makers, S.A. de C.V.
2024-09-20
OASIS
OASIS
98736747 not registered Live/Pending
Oasis Hill, LLC
2024-09-06
OASIS
OASIS
98736716 not registered Live/Pending
Oasis Hill, LLC
2024-09-06
OASIS
OASIS
98730414 not registered Live/Pending
Oasis Distillery LLC
2024-09-03
OASIS
OASIS
98698250 not registered Live/Pending
Ecolab USA Inc.
2024-08-14
OASIS
OASIS
98610582 not registered Live/Pending
AMERICAN HEALTH SERVICE SALES CORPORATION
2024-06-20
OASIS
OASIS
98608981 not registered Live/Pending
AEG International, LLC
2024-06-19
OASIS
OASIS
98605667 not registered Live/Pending
JASON RIVER
2024-06-17
OASIS
OASIS
98605590 not registered Live/Pending
JASON RIVERS
2024-06-17
OASIS
OASIS
98559772 not registered Live/Pending
ePlant, Inc.
2024-05-20
OASIS
OASIS
98527307 not registered Live/Pending
Wolf Steel Group Inc.
2024-04-30
OASIS
OASIS
98507202 not registered Live/Pending
OASIS SECURITY LTD
2024-04-18

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.