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Variants of LIQUIFILM by Allergan Sales, LLC
4 variants
Key
Device
Device · Manufacturer · Authorizations
Verified
Verified
Status
Status
Regime
Regime
Registry
Registry
Class
Class
Liquifilm
UDI-DI 10840228300820
Allergan Sales, LLC
·
,
United States
CE/MDR
3829879CE01
Expiring
Valid to May 2027
Expiring
Regimes:
CE MDR
Registry:
EUDAMED
Class
Class:
IIb
Liquifilm
UDI-DI 10840228300813
Allergan Sales, LLC
·
,
United States
CE/MDR
3829879CE01
Expiring
Valid to May 2027
Expiring
Regimes:
CE MDR
Registry:
EUDAMED
Class
Class:
IIb
Liquifilm
UDI-DI 10840228300806
Allergan Sales, LLC
·
,
United States
CE/MDR
3829879CE01
Expiring
Valid to May 2027
Expiring
Regimes:
CE MDR
Registry:
EUDAMED
Class
Class:
IIb
Liquifilm
UDI-DI 10840228302534
Allergan Sales, LLC
·
,
United States
CE/MDR
3829879CE01
Expiring
Valid to May 2027
Expiring
Regimes:
CE MDR
Registry:
EUDAMED
Class
Class:
IIb
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