← Back to catalogue

Bmet-11, F/G

FDA UDI

Class II (US FDA UDI)

by Ranfac Corp.

Identity

Trade Name
BMET-11, F/G FDA UDI
Generic Name
Bone marrow biopsy procedure kit FDA UDI
Device Name
TRAY, BMET-11, F/G PN 74076-01M FDA UDI
Model / Reference
11 Gauge x 4" FDA UDI
Description
TRAY, BMET-11, F/G PN 74076-01M FDA UDI

Identifiers

Catalog Number
BMET-11 FDA UDI
Primary DI / UDI-DI
M9797407601M0 FDA UDI
510(k) Number
K983187 FDA UDI
FDA Product Code
KNW FDA UDI
GMDN Term
Bone marrow biopsy procedure kit 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

Yes

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
Needle Gauge — 11 Gauge FDA UDI
Length — 4 Inch FDA UDI

Category: Bone marrow biopsy procedure kit

Bmet-11, F/G by Ranfac Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone marrow biopsy procedure kit.

Cleared under the same submission

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

Manufacturer
Ranfac Corp.

Sources (1)

  • FDA UDI 7eaa5519-fc0a-49b8-b6c2-e84473c9743b 37 fields · synced Jun 6, 2026