PlastiBell Circumcision Device

GUDID 00840113231638

1.2 cm PlastiBell Circumcision Device

ASPEN SURGICAL PRODUCTS, INC.

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Primary Device ID00840113231638
NIH Device Record Keya24e03d3-c33d-4f61-814d-80071557e675
Commercial Distribution StatusIn Commercial Distribution
Brand NamePlastiBell Circumcision Device
Version Model Number9232
Company DUNS027680821
Company NameASPEN SURGICAL PRODUCTS, 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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100840113231638 [Primary]

FDA Product Code

FHGBell, circumcision

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-03-07
Device Publish Date2023-02-27

On-Brand Devices [PlastiBell Circumcision Device]

008401132316761.7 cm PlastiBell Circumcision Device
008401132316691.5 cm PlastiBell Circumcision Device
008401132316521.4 cm PlastiBell Circumcision Device
008401132316451.3 cm PlastiBell Circumcision Device
008401132316381.2 cm PlastiBell Circumcision Device
008401132316211.1 cm PlastiBell Circumcision Device
00840113231614PlastiBell Circumcision Device, Physician Bulk Pack
008401132316071.7 cm PlastiBell Circumcision Device
008401132315911.5 cm PlastiBell Circumcision Device
008401132315841.4 cm PlastiBell Circumcision Device
008401132315771.3 cm PlastiBell Circumcision Device
008401132315601.2 cm PlastiBell Circumcision Device
008401132315461.1 cm PlastiBell Circumcision Device
00840113231539PlastiBell Circumcision Device, Hospital Bulk Pack

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