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Dannik

FDA UDI

Class II (US FDA UDI)

by Dannik LLC

Identity

Trade Name
Dannik FDA UDI
Generic Name
Endoscopic electrosurgical handpiece/electrode, monopolar, single-use FDA UDI
Device Name
Disposable Monopolar 5mm x 33cm Autraumatic Fenestrated Grasper, Ratcheting FDA UDI
Model / Reference
DMP5920 FDA UDI
Description
Disposable Monopolar 5mm x 33cm Autraumatic Fenestrated Grasper, Ratcheting FDA UDI

Identifiers

Primary DI / UDI-DI
10850013527042 FDA UDI
510(k) Number
K193019 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Endoscopic electrosurgical handpiece/electrode, monopolar, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic electrosurgical handpiece/electrode, monopolar, single-use

Dannik by Dannik LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic electrosurgical handpiece/electrode, monopolar, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dannik LLC

Sources (1)

  • FDA UDI 6e82e278-c0cb-4124-afef-abf6836a73dd 34 fields · synced Jun 8, 2026