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Rtn-116-T

FDA UDI

Class II (US FDA UDI)

by Ranfac Corp.

Identity

Trade Name
RTN-116-T FDA UDI
Generic Name
Bone marrow biopsy needle, single-use FDA UDI
Device Name
NEEDLE, RTN-116-T, F/G, STERILE, RANFAC P/N 74424-01M FDA UDI
Model / Reference
11 GA X 6 IN FDA UDI
Description
NEEDLE, RTN-116-T, F/G, STERILE, RANFAC P/N 74424-01M FDA UDI

Identifiers

Catalog Number
RTN-116-T FDA UDI
Primary DI / UDI-DI
00850023741820 FDA UDI
510(k) Number
K983187 FDA UDI
FDA Product Code
KNW FDA UDI
GMDN Term
Bone marrow biopsy needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1075 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

No

FDA UDI

Dimensions & Sizes

Size
Length — 6 Inch FDA UDI
Needle Gauge — 11 Gauge FDA UDI

Category: Bone marrow biopsy needle, single-use

Rtn-116-T by Ranfac Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone marrow biopsy needle, 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
Ranfac Corp.

Sources (1)

  • FDA UDI 8b389096-4b07-4757-bd01-569f68ddc949 37 fields · synced May 30, 2026