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Basic

FDA UDI

Class II (US FDA UDI)

by Dannik LLC

Identity

Trade Name
BASIC FDA UDI
Generic Name
Tissue extraction bag FDA UDI
Device Name
Basic Specimen Retrieval Bag, 240mL FDA UDI
Model / Reference
NS0240 FDA UDI
Description
Basic Specimen Retrieval Bag, 240mL FDA UDI

Identifiers

Primary DI / UDI-DI
10850013527677 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Tissue extraction bag FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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
MRI Safety
MR Unsafe FDA UDI

Category: Tissue extraction bag

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

Similar devices

Also classified as Tissue extraction bag.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dannik LLC

Sources (1)

  • FDA UDI cc116805-23a1-49f8-9353-7ebe2af113c8 33 fields · synced Jun 8, 2026