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Results for “MIASPAS”
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EUDAMED
79
FDA 510(k)
1
FDA PMA
GUDID
87
Country / market
European Union (all)
55
United States
88
More countries (1)
Germany
55
Risk class
Class I
80
Class IIa
10
Class IIb
Class III
Class II (US)
2
More classes (11)
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IVD Annex II List A
IVD Annex II List B
IVD for self-testing
Active implantable (AIMDD)
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92 devices found
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Device · Manufacturer · Authorizations
Verified
Status
Regime
Registry
Class
Miaspas BV175S
Aesculap, Inc.
·
,
FDA registration: United States
Class II
GUDID
not on market
Withdrawn
GUDID
II
Miaspas Mini-Tta FG051R
Aesculap, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Miaspas FG894R
Aesculap, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Miaspas FG914R
Aesculap, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Miaspas FG912R
Aesculap, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Miaspas Mini-Alif FF895R
Aesculap, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Miaspas FW819R
Aesculap, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Miaspas Mini-Alif FD085R
Aesculap, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Miaspas FG904R
Aesculap, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Miaspas FG902R
Aesculap, Inc.
·
,
FDA registration: United States
Class I
GUDID
not on market
Withdrawn
GUDID
I
Miaspas Minitta Anterior Micro Surgical Transthoracic Approach Instrumentation
Aesculap, Inc.
·
,
FDA registration: United States
Class II
FDA 510(k)
K003740
Active
Cleared 27 Apr 2001
Active
510(k)
510(k)
II
Miaspas
UDI-DI 04038653153190
Aesculap AG
·
,
Germany
Class I
CE/MDR
Active
CE MDR
EUDAMED
I
4 variants
See all variants of this device
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Showing 81-92 of 92