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Aesculap, product family

by Aesculap AGand 1 other manufacturer record 14 variants Basic UDI-DI 40392390000003922D

Shared by every variant

Manufacturer
Aesculap AG(12)AESCULAP, INC.(2)
Several manufacturer records share this Basic UDI-DI.
Basic UDI-DI
40392390000003922D
Risk class
Class I
Legislation
MDR
EMDN category
NASAL AND PARANASAL CAVITY SURGERY PLIERS, REUSABLE
Market status
14 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 40392390000003922D.

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 14 devices listed on this page; other pages of the family can carry others.

Variants

14 devices · page 1 of 1

Variants of Aesculap, Basic UDI-DI 40392390000003922D
UDI-DISize and differences
Aesculap
Aesculap AG
OK505R04038653177257 —On the market
Aesculap
Aesculap AG
OK506R04038653177264 —On the market
Aesculap
Aesculap AG
OK507R04038653177271 —On the market
Aesculap
Aesculap AG
OK508R04038653177288 —On the market
Aesculap
Aesculap AG
OK520R04038653177301 —On the market
Aesculap
Aesculap AG
OK521R04038653177325 —On the market
Aesculap
Aesculap AG
OK522R04038653177332 —On the market
Aesculap
Aesculap AG
OK525R04038653052622 —On the market
Aesculap
Aesculap AG
OK526R04038653177349 —On the market
Aesculap
Aesculap AG
OK527R04038653177356 —On the market
Aesculap
Aesculap AG
OK529R04038653177363 —On the market
Aesculap
Aesculap AG
OK530R04038653177370 —On the market
AESCULAP OK509R
AESCULAP, INC.
OK509R / OK509R04038653177295 —On the market
AESCULAP OK531R
AESCULAP, INC.
OK531R / OK531R04038653177387 —On the market