DEVICE: Bioseal Inc. (00630094177717)

Device Identifier (DI) Information

Bioseal Inc.
17771/100
In Commercial Distribution

BIOSEAL
00630094177717
GS1

1
186968939 *Terms of Use
Plastic Ampule Breaker
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Device Characteristics

Labeling does not contain MRI Safety Information
No
No
Yes
No
No
No
No
No

GMDN

[?]

GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.

GMDN Term Code GMDN Term Name GMDN Term Definition GMDN Term Status [?] Implantable?
10098 Ampule opener
A cutting instrument intended to safely remove/break the protective, sterile seal of an ampule. It is typically designed to protect the user from inadvertent contact with the sharp edges of the seal while being removed. This is a reusable device.
Active false
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FDA Product Code

[?]
Product Code Product Code Name
KDC INSTRUMENT, SURGICAL, DISPOSABLE
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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
Premarket Submission Number Not Available/Not Released
Yes CLOSE

Sterilization

Yes
No
Sterilization Method [?]
No Sterilization Methods Found
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Storage and Handling

[?]
Storage and Handling
No storage/handling found
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Clinically Relevant Size

[?]
Size Type Text
No Device Sizes
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Device Record Status

9cf746df-732a-46fd-8bb3-796f223e3876
October 11, 2023
1
October 03, 2023
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Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]
Package DI Number Quantity per Package Contains DI Package Package Discontinue Date Package Status Package Type
10630094177714 100 00630094177717 In Commercial Distribution Case
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Secondary DI

[?]
Issuing Agency [?] Secondary DI Number
No Secondary DIs found
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Unit of Use DI

[?]
Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]
Yes
No
None
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Production Identifier(s) in UDI

[?]
Yes
No
No
Yes
No CLOSE

Customer Contact

[?]
No Customer Contact currently defined
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