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nubert

FDA UDI

Class II (US FDA UDI)

by Vernacare Limited

Identity

Trade Name
nubert FDA UDI
Generic Name
Tissue extraction bag FDA UDI
Device Name
Impervious, assymetric bag for the endoscopic retrieval of tissue. Volume 100 mL. Port size 10 mm. FDA UDI
Model / Reference
24003US FDA UDI
Description
Impervious, assymetric bag for the endoscopic retrieval of tissue. Volume 100 mL. Port size 10 mm. FDA UDI

Identifiers

Catalog Number
24003US FDA UDI
Primary DI / UDI-DI
05019829239923 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

No

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

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 100 Milliliter FDA UDI

Category: Tissue extraction bag

nubert by Vernacare Limited — 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
Vernacare Limited

Sources (1)

  • FDA UDI 404d352e-31ff-4d67-bc4f-26f37c0c7ff9 37 fields · synced Jun 6, 2026