← Back to catalogue

NOVO Health Services, LLC

FDA UDI

Class II (US FDA UDI)

by Novo Health Services, Llc

Identity

Trade Name
NOVO Health Services, LLC FDA UDI
Generic Name
Sterilization packaging, single-use FDA UDI
Device Name
GreenWrap 48x48", 20-Pk NS FDA UDI
Model / Reference
124675 FDA UDI
Description
GreenWrap 48x48", 20-Pk NS FDA UDI

Identifiers

Catalog Number
124675B FDA UDI
Primary DI / UDI-DI
00810019800658 FDA UDI
510(k) Number
K102783 FDA UDI
FDA Product Code
FRG FDA UDI
GMDN Term
Sterilization packaging, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Height — 6 Inch FDA UDI
Width — 24 Inch FDA UDI
Weight — 18.5 Pound FDA UDI

NOVO Health Services, LLC by Novo Health Services, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 9b43f629-c718-4ecb-9e51-51c4ae253b72 38 fields · synced May 30, 2026