Primary Device ID | 00840113231614 |
NIH Device Record Key | 345393da-587a-44dc-b505-f9bc4e1f2181 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PlastiBell Circumcision Device |
Version Model Number | 9230 |
Company DUNS | 027680821 |
Company Name | ASPEN SURGICAL PRODUCTS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840113231614 [Primary] |
FHG | Bell, circumcision |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-03-07 |
Device Publish Date | 2023-02-27 |
00840113231676 | 1.7 cm PlastiBell Circumcision Device |
00840113231669 | 1.5 cm PlastiBell Circumcision Device |
00840113231652 | 1.4 cm PlastiBell Circumcision Device |
00840113231645 | 1.3 cm PlastiBell Circumcision Device |
00840113231638 | 1.2 cm PlastiBell Circumcision Device |
00840113231621 | 1.1 cm PlastiBell Circumcision Device |
00840113231614 | PlastiBell Circumcision Device, Physician Bulk Pack |
00840113231607 | 1.7 cm PlastiBell Circumcision Device |
00840113231591 | 1.5 cm PlastiBell Circumcision Device |
00840113231584 | 1.4 cm PlastiBell Circumcision Device |
00840113231577 | 1.3 cm PlastiBell Circumcision Device |
00840113231560 | 1.2 cm PlastiBell Circumcision Device |
00840113231546 | 1.1 cm PlastiBell Circumcision Device |
00840113231539 | PlastiBell Circumcision Device, Hospital Bulk Pack |