Dynamic DIAGNOSTICS, INC

FDA UDI

Class II (US FDA UDI)

by Bioprotech Inc.

Identity

Trade Name: Dynamic DIAGNOSTICS, INC FDA UDI
Generic Name: Electrosurgical return electrode, single-use FDA UDI
Device Name: Horizontal, Non-corded, Adult or Pediatric, Split, 150x120mm, Foam, 5pcs per pouch FDA UDI
Model / Reference: 9552F FDA UDI
Description: Horizontal, Non-corded, Adult or Pediatric, Split, 150x120mm, Foam, 5pcs per pouch FDA UDI

Identifiers

Primary DI / UDI-DI: 00851255007159 FDA UDI
510(k) Number: K073360 FDA UDI
FDA Product Code: GEI FDA UDI
GMDN Term: Electrosurgical return electrode, 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Electrosurgical return electrode, single-use

Dynamic DIAGNOSTICS, INC by Bioprotech Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K073360 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Bioprotech Inc.

Sources (1)

FDA UDI 236aae89-1db0-4252-a843-61e2d4d4e640 35 fields · synced May 31, 2026